AstraZeneca

<div>JOB TITLE
 Senior MSL &ndash; Rare Diseases (Haematology, Nephrology and Transplant) 
ABOUT ASTRAZENECA
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world&rsquo;s most serious diseases. But we&rsquo;re more than one of the world&rsquo;s leading pharmaceutical companies.
SITE DESCRIPTION
AstraZeneca is experiencing a significant transformation in the Kingdom of Saudi Arabia, driven by a commitment to advancing healthcare, innovation, and sustainable growth. Building on our global legacy, AZ KSA is rapidly evolving its operations to better serve patients, collaborate with healthcare stakeholders, and contribute to the ambitious goals outlined in the Saudi Vision 2030. We are investing in talent, digital solutions, and new ways of working; all designed to enhance our impact on patient outcomes and reinforce our leadership in therapeutic areas. This dynamic environment calls for visionary, agile professionals who thrive in change and are motivated to help shape the future of healthcare in KSA.
ROLE SUMMARY
AstraZeneca is accelerating the expansion of our geographical footprint in rare diseases following the acquisition of Alexion in 2021. Rare disease is a high-growth therapy area with rapid innovation and significant unmet medical need. Over 7,000 rare diseases are known today &ndash; yet less than 1% of them have an approved treatment.
As we build our position as a Rare Disease leader, we seek a Rare Disease Medical Science Liaison to join our Medical Affairs team in Western Region, KSA.
As a Medical Science Liaison &ndash; Rare Disease you'll play a pivotal role in channelling our scientific capabilities to bring an important new therapy in a rare disease setting into clinical practice, making a positive impact on patients' lives.
The Medical Science Liaison &ndash; Rare Disease is a professional with scientific, clinical and therapeutic area expertise responsible for providing medical and scientific support to healthcare professionals aligned to the use of medicines in our combined rare disease portfolio. You will report into the Medical Manager Rare Disease.
In this role you will be expected to identify and cultivate relationships with HCPs working in the field including physicians, nurse practitioners, registered nurses and pharmacists as well as other key strategic partners, such as patient advocacy groups. You will conduct educational programs on disease state and the appropriate use of our medicines, consistent with Medical Affairs plans and objectives. You will also respond to customer inquiries to ensure focused clinical and scientific information that supports the appropriate use of these medicines.
Additionally you will deliver clinical and scientific information to support appropriate use of the medicine in the relevant therapy area in a patient focused manner; maintain expertise in disease state management, keep abreast of emerging therapies and the therapeutic landscape; gather customer insights regarding the use of the medicine in the wider therapeutic landscape to help inform medical and commercial strategies while adhering to internal standards, processes and complying with regulatory and compliance requirements.
What you&rsquo;ll do
Advanced Stakeholder Engagement<ul><li>
Provide AZ with an understanding of the local medical community, clinical practice trends, HCP insight and real or perceived gaps in current scientific knowledge and medical treatment</li><li>
Share emerging data with HCPs, discussing all aspects of the data in a scientific, objective, and balanced way.
</li><li>Responsible for identifying and developing scientifically based relationships with KEEs.</li><li>
Work with HCPs as partners in scientific activities that help advance disease understanding and are consistent with Medical Affairs strategy &amp; objectives, such as:<ul><li>
Interact in the field with the medical community in the context of various medical projects such as clinical trials, Non-Interventional Studies, Investigator Sponsored Studies (ISSs), scientific exchange.</li><li>
 Identify potential speakers and train speakers as appropriate for local events</li><li>
Provide recommendations for advisory board/Round Table discussion participants and serve as faculty/facilitators for advisory board meetings.</li><li>
Present scientific data to HCPs in both group (Medically led meetings) and one on one setting.</li><li>
Facilitate continuing medical education events for HCPs.</li></ul></li></ul>
Develop or initiate scientific programs to explore unmet medical needs in priority disease area(s) through obtaining and sharing valuable insights<ul><li>
Provide actionable insights that enhance the value and appropriate use of AZ products and disease management to internal stakeholders</li><li>
Engage in strategic planning meetings with payer customers or hospital decision makers where the discussion of scientific topics is clearly separated from discussion of promotional and/or other business topics.</li><li>
Demonstrate expertise and knowledge of AZ products, emerging therapies, competitors, patient and treatment trends, clinical trials, and scientific activities within the Disease Area and continuously updates this expertise and knowledge based on training direction and approved resources provided.</li><li>
Support the Medical Manager and Marketing Team in development of non-promotional and promotional materials/programs.</li></ul>
Act as scientific expert in priority disease area for internal stakeholders<ul><li>
Continuously acquire and update necessary scientific knowledge on therapeutic area and relevant compounds.</li><li>
Provide the AZ internal stakeholders with an understanding of the local medical community, clinical practice, trends and real or perceived gaps in current scientific knowledge and medical treatment, competitor information</li><li>
Provide scientific support at AZ sponsored educational events</li><li>
Gather, monitor, and share competitor knowledge that may affect company strategies</li><li>
Planning and executing regional medical activities during the product launch processes.</li></ul>
Medical Background Training<ul><li>
Serve as a medical resource for the sales representatives and accurately answer any medical question they may have to help them utilize their approved materials and to help them understand therapeutic area.</li><li>
Participate/develop/conduct therapeutic area and product trainings and periodic scientific updates to the internal customers</li></ul>
Medical Information<ul><li>
Respond to unsolicited requests for information about unapproved AZ products or unapproved uses of approved products, presenting such information in an objective, well balanced, substantiated manner that is scientific in tone and content, free of promotional messages, truthful, and is not misleading</li></ul>
Demonstrate appropriate response and documents the provision of accurate, scientific data in response to unsolicited scientific questions posed by Healthcare providers with Company Policies, and applicable laws, regulations, and ethical standards.
Essential for the role<ul><li>
Bachelor&rsquo;s degree in Medicine, Pharmacy, or Pharmacology</li><li>
Minimum of 2 years&rsquo; experience in Medical Affairs and at least 6 years within the pharmaceutical industry</li><li>
Proven ability to synthesize complex scientific information and communicate effectively with healthcare professionals at a peer level</li><li>
Strong aptitude for learning and applying scientific concepts and knowledge</li><li>
Experience in Hematology, Oncology, Nephrology, Rare Diseases, and/or Critical Care is highly desirable</li><li>
Direct patient care experience or equivalent experience within the pharmaceutical industry is preferred</li><li>
Excellent presentation skills, with the ability to clearly communicate medical data and concepts</li><li>
Proficiency in Microsoft Office applications (Excel, Word, PowerPoint, etc.)</li><li>
Strong project management skills</li><li>
Excellent written and verbal communication, with strong interpersonal abilities</li><li>
Demonstrated leadership capabilities and the ability to work independently</li></ul>
Why AstraZeneca?
At AstraZeneca we&rsquo;re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There&rsquo;s no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth, and development. We&rsquo;re on an exciting journey to pioneer the future of healthcare. 
So, what&rsquo;s next?
<ul><li>Are you already imagining yourself joining our team? Good, because we can&rsquo;t wait to hear from you.</li><li>
Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it&rsquo;s yours.</li></ul>
Where can I find out more?
Our Social Media, Follow AstraZeneca on LinkedIn
Follow AstraZeneca on Facebook
Follow AstraZeneca on Instagram</div>

Senior MSL Rare Disease

CIBC

<div>We&rsquo;re building a relationship-oriented bank for the modern world. We need talented, passionate professionals who are dedicated to doing what&rsquo;s right for our clients.
At CIBC, we embrace your strengths and your ambitions, so you are empowered at work. Our team members have what they need to make a meaningful impact and are truly valued for who they are and what they contribute.
To learn more about CIBC, please visit CIBC.com
As a Private Banking MSL Team - Business Effectiveness Coordinator, you will actively lead and support various projects while collaborating closely with Private Bankers to deliver exceptional service to High Net Worth and Ultra High Net Worth clients within our Marketable Secured Lending space. You will serve as a key liaison among clients, Bankers, Wealth Advisors, and internal Operations teams to ensure that all Securities Based Product requests are processed accurately and efficiently. Your responsibilities include verifying the credit application is correct, preparing the file for document preparation/closing, and tracking loan documentation, maintaining and organizing client files, and managing the full lifecycle of account openings and closures. Additionally, you will assist clients with research inquiries and document collection, oversee complex money movements such as advances, payments, ACH transactions, loan draws, and wires, and conduct thorough billing reviews for accuracy. You will also contribute to reporting processes and proactively address and resolve any exceptions to ensure seamless operations.
At CIBC we enable the work environment most optimal for you to thrive in your role. You&rsquo;ll have the flexibility to manage your work activities within a hybrid work arrangement where you&rsquo;ll spend 3-4 days per week on-site, while other days will be remote.
How You&rsquo;ll Succeed<ul><li>
Client Service: Providing high-touch and top-tier client service related to MSLs for Private Banking clients and advisors by working with a sense of urgency and accuracy to finalize loan documentation and booking. You will be asked to assist clients with research inquiries and document collection, providing timely and thorough support.</li></ul><ul><li>
Risk reviews: Proactively respond to any inquiries, and stay up-to-date on the latest tools and information that can help reduce our operational risk and provide top-tier client service. Relationship building &ndash; Listen, ask questions, and truly understand the business. Deepen your relationship with business partners by using your knowledge of their team when working with partners. Use your professional network to escalate any challenges to the executive level in a constructive and effective way.</li><li>
Governance support: Contribute to governance oversight providing requested documentation and/or answer questions as posed.</li></ul><ul><li>
Comprehensive Analysis: Work closely with our Private Bankers and Wealth Advisors to ensure a timely and accurate experience for our Clients throughout the entire process. You will provide comprehensive project management and support, actively contributing to the planning, execution, and successful completion of key initiatives.</li><li>
High-Quality Decision-Making: Responsible for ensuring all file documentation is complete, accurate, verified and meets set deadlines. You will oversee the end-to-end process of account openings and closures, ensuring accuracy and a positive client experience.</li><li>
Effective Risk Assessment: Ensure processes align with the bank&rsquo;s guidelines, risk appetite, policies, and consumer laws and regulation requirements while providing sound judgment. You will analyze and review billing statements for accuracy, identifying and resolving discrepancies proactively.</li></ul><ul><li>
Strong Written Communication: Craft detailed communication that clearly present rationale, assessment, and evaluation results. You will prepare and review loan files for document preparation, meticulously tracking executed documents to ensure timely and accurate booking.</li><li>
Collaboration &amp; Stakeholder Engagement: Work closely with all key stakeholders: Securities Based Lending Team, Private Bankers, Wealth Advisors, Underwriters, Closers, Post Closers, Group Portfolio Managers, and Senior Management to ensure seamless loan/line processing and deliver exceptional sales support and service to High Net Worth and Ultra High Net Worth clients.</li><li>
Market Awareness &amp; Compliance: Stay updated on market conditions, industry regulations, and consumer lending laws to maintain compliance and adapt to evolving enhancements. You will maintain and organize client folders, guaranteeing proper storage and adherence to compliance standards.</li><li>
Community Involvement: Complete at least five community outreach volunteer hours annually, contributing to the bank&rsquo;s commitment to community development.</li></ul>
Who You Are<ul><li>
You demonstrate experience in in Securities Back Lending or Private Banking or Wealth. It&rsquo;s an asset if you have least 5 years of experience in on wealth-high net worth lending with a strong grasp of risk assessment for high-net-worth clients.</li><li>
You have a degree/diploma in finance, or a related field.</li><li>
You give meaning to data.. You have strong problem-solving skills, can identify and quantify problems, and provide effective resolutions. You communicate detailed information in a meaningful way. You can analyze credit reports, assets, and liabilities with expertise in loan opening, processing, and pre-closing tasks.</li><li>
You know that details matter. You notice things that others don't. Your critical thinking skills help to inform your decision-making</li><li>
You are a strong communicator. You excel at verbal and written communication, clearly presenting information to stakeholders, including assisting with procedural/job aid updates, and presentation materials for training. This includes supporting department special projects and/or testing initiatives.</li><li>
You can demonstrate experience in industry tools and systems like Supernova, FastNet,, MS Office (Excel, Word, PowerPoint, Teams, Outlook) products, and FIS/IBS.</li><li>
You have regulatory Knowledge. You have a strong understanding of federal and state lending regulations, ensuring compliance with consumer protection laws.</li><li>
You're motivated by collective success. You know that teamwork can transform a good idea into a great one. You know that an inclusive team that enjoys working together can bring a vision to life.</li><li>
Values matter to you. You bring your real self to work and you live our values - trust, teamwork, and accountability.</li></ul>
California residents &mdash; your privacy rights regarding your actual or prospective employment
At CIBC, we offer a competitive total rewards package. This role has an expected salary range of $70,000 - $80,000 for the market based on experience, qualifications, and location of the position. The successful candidate may be eligible to participate in the relevant business unit&rsquo;s incentive compensation plan, which may also include a discretionary bonus component. CIBC offers a full range of benefits and programs to meet our employee&rsquo;s needs; including Medical, Dental, Vision, Health Savings Account, Life Insurance, Disability, and Other Insurance Plans, Paid Time Off (including Sick Leave, Parental Leave and Vacation), Holidays and 401(k), in addition to other special perks reserved for our team members.
This position does not offer visa sponsorship.
#LI-TA
What CIBC Offers
At CIBC, your goals are a priority. We start with your strengths and ambitions as an employee and strive to create opportunities to tap into your potential. We aspire to give you a career, rather than just a paycheck.<ul><li>
We work to recognize you in meaningful, personalized ways including a competitive salary, incentive pay, banking benefits, a benefits program*, a vacation offering, wellbeing support, and MomentMakers, our social, points-based recognition program.</li><li>
Our spaces and technological toolkit will make it simple to bring together great minds to create innovative solutions that make a difference for our clients.</li><li>
We cultivate a culture where you can express your ambition through initiatives like Purpose Day; a paid day off dedicated for you to use to invest in your growth and development.</li></ul><ul><li>Subject to plan and program terms and conditions</li></ul>
What you need to know<ul><li>
CIBC is committed to creating an inclusive environment where all team members and clients feel like they belong. We seek applicants with a wide range of abilities and we provide an accessible candidate experience. If you need accommodation, please contact Mailbox.careers-carrieres@cibc.com</li><li>
You need to be legally eligible to work at the location(s) specified above and, where applicable, must have a valid work or study permit.</li><li>
We may ask you to complete an attribute-based assessment and other skills tests (such as simulation, coding, MS Office). Our goal for the application process is to get to know more about you, all that you have to offer, and give you the opportunity to learn more about us.</li></ul>
Job Location
IL-120 S LaSalle St, 3rd Fl
Employment Type
Regular
Weekly Hours
40
Skills
Analytical Thinking, Enterprise Risk Management (ERM), Group Problem Solving, Reporting and Analysis, Risk Assessments, Risk Monitoring, Teamwork</div>

Private Banking MSL Team - Business Effectiveness Coordinator

Johnson & Johnson

<div>At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.
As guided by Our Credo, Johnson &amp; Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson &amp; Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Medical Affairs Group
Job Sub Function:
Medical Science Liaison
Job Category:
Scientific/Technology
All Job Posting Locations:
Austin, Texas, United States, SAN ANTONIO, Texas, United States of America
Job Description:
Johnson &amp; Johnson Innovative Medicines is recruiting for a Medical Science Liaison, Immunology - Dermatology to be based in Central Texas, which includes San Antonio and Austin, TX.
About Immunology
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses. You can influence where medicine is going by restoring health to millions of people living with immune diseases.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Learn more at https://www.jnj.com/innovative-medicine
The Medical Science Liaison (MSL) is responsible for providing fair balanced, objective, scientific information and education to opinion leaders (OLs), health care professionals, and to internal partners as required by scientific and business needs. The MSL is considered a scientific and clinical knowledge lead on current and future J&amp;J Innovative Medicine products per Therapeutic Area (TA) alignment. The MSL is responsible for staying abreast of current scientific and treatment landscape trends in their therapeutic areas of interest. The MSL provides research support for company and investigator initiated research.
The MSL will function with high integrity and follow credo values. The MSL is responsible for building external relationships with identified OLs and health care providers (MD, PA, NP, RN, Pharm.D., biocoordinators) and developing and managing a geographical territory. These relationships and engagements can include both virtual &amp; in-person, with a prioritization of in-person engagements when appropriate. The MSL is responsible for developing and maintaining a territory strategic plan, which includes educational activities with identified OLs, HCPs, institutions, and community practices. The MSL will be expected to rapidly identify and compliantly collaborate with field based partners to ensure support of the Healthcare Providers which will positively impact the patients that they care for.
The MSL will continue to enhance their skills and agility, applying the competencies of Change Management, Time Management and Innovation. The MSL is responsible for conducting all activities in accordance with current regulatory and health care compliance guidelines.
This is a field based clinical position which required travel, primarily throughout assigned geography, with infrequent meeting travel outside of assigned geography. Travel for this role is estimated at 60%
Summary:
Consistently demonstrate strategic territory planning and ability to build strong relationships within the territory:<ul><li>
Responsible for developing and maintaining a field strategic plan</li><li>
Responds in a timely manner to unsolicited scientific inquiries of HCPs/investigators/health care systems/academic medical centers and population health decision makers integrating scientific data including real world evidence into real life practice to meet customer needs</li><li>
Presents data and information in a manner appropriate to the audience and request.</li><li>
Execute plans regarding reactive and proactive outreaches as approved via the legal/HCC exceptions process</li><li>
Prioritize franchise customer-based initiatives and field responsibilities, while balancing administrative duties and project responsibilities.</li></ul>
Executes Research Initiatives:<ul><li>
Engages with external investigators regarding unsolicited research inquiries and act as liaison to R&amp;D, Medical Affairs and operations teams</li><li>
Provides clinical trial support to identify potential sites, resolve issues with enrolled sites, and participate in meetings as appropriate, including site initiation visits and investigator launch meetings.</li></ul>
Consistently demonstrates strong scientific acumen:<ul><li>
Actively participate in team calls, trainings, &amp; journal clubs through scientific dialogue, and regularly sharing of scientific news.</li><li>
Attends scientific conferences to gather and understand new scientific information relevant to the company and the external scientific community</li><li>
Medical insights: Actively listens for, documents, and shares medical insights.</li><li>
Sets aside time for self-driven learnings on current scientific landscape</li><li>
Role include representing and supporting JNJ at relevant scientific or other key stakeholder meetings including congresses, symposia, advisory boards and investigator meetings</li><li>
Role includes representing JNJ at speaking engagements at relevant scientific or other key stakeholder meetings</li></ul>
Continuously support Department Operations and Internal Partners:<ul><li>
Performs all administrative requirements in a timely, accurate and compliant manner (e.g. expense reports, documentation of activities)</li><li>
Maintain focus and composure in uncertain circumstances with minimal direction.</li><li>
Provide regional and local support to enhance sales training initiatives and improve competencies of field personnel in partnership with Sales Learning and Development</li><li>
Communicates and collaborates with all field based partners, and other Immunology MSL teams on a routine basis.
</li><li>Fully understands and applies MSL SOP's/guidelines and company HCC/Regulatory/Legal guidelines.</li></ul>
Qualifications:
PharmD, PhD, MD, or other advanced medical degree, NP (Nurse Practitioner), PA (Physician Assistant)), with 2+ years relevant TA clinical experience
Ability to support travel up to 60-70% which includes overnight travel, including some weekend commitments
Ability to drive to or fly to various meetings/congresses/headquarters
A valid U.S. driver&rsquo;s license and clean driving record
Reside within the defined assigned territory
Preferred:
A preference of 2+ years relevant work experience including clinical, research, fellowship, or pharmaceutical work experience with presentation skills
Knowledge or experience in the relevant TA and/or Immunology work experience
Must be familiar with Microsoft Word, Excel, PowerPoint, and utilization of computers and remote technologies
Reside in or near San Antonio and Austin, TX.
Johnson &amp; Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson &amp; Johnson is committed to providing an interview process that is inclusive of our applicants&rsquo; needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers and internal employees contact AskGS to be directed to your accommodation resource.
Required Skills:
Preferred Skills:
Analytics Dashboards, Clinical Research and Regulations, Clinical Trials, Coaching, Critical Thinking, Customer Centricity, Data-Driven Decision Making, Data Reporting, Digital Culture, Digital Literacy, Medical Affairs, Medical Communications, Medical Compliance, Organizing, Product Knowledge, Relationship Building, Research and Development, Strategic Thinking, Technical Credibility</div>

Medical Science Liaison - Dermatology (Central Texas)

Bristol Myers Squibb

<div>Working with Us 
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. 
 
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . 
 
MSL Position Summary 
 
MSLs embody our medical mission in becoming a trusted, agile partner who engages in relevant dialogue and delivers timely, high impact data and insights that advance the science or accelerate access, optimize medical practice and drive appropriate adoption of BMS medicines. The MSL role is a field-based role and it is anticipated that a MSL will spend their time in the field with external customers. 
 
The primary role of MSLs is to develop and maintain contacts with Thought Leaders (TL) and Healthcare Providers (HCP) within their healthcare system. The purpose of interactions is to ensure patients have access to BMS medicines, to ensure their safe and appropriate use through peer-to-peer discussions aligned with medical strategies and needs expressed by the stakeholders. The scientific dialogue focuses on scientific/clinical information around disease management and BMS products in a fair and balanced way and includes appropriate Health Economics and Outcomes Research (HEOR) data. 
 
Position Responsibilities 
 
1. External Environment and Customer Focus
 
 
<ul><li>Develop and maintain interactions with Thought Leaders, appropriate HCPs, and access stakeholders, within a given geography to answer scientific, unsolicited product and HEOR related questions. MSLs will use various channels for interactions (1:1, group presentation; remote, etc.).</li></ul> 
<ul><li>Effectively present information to HCPs and be able to respond to questions, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives.</li></ul> 
<ul><li>Actively assess the medical landscape by meeting with Thought Leaders to understand their needs and expertise. Continuously update own knowledge in treatment strategies, products, unmet medical needs, clinical trials and scientific activities. Understand the competitive landscape and actively prepare to address informational needs of customers.</li></ul> 
<ul><li>Collect and provide meaningful medical insights back to the medical and commercial organization to be actioned in support of the strategy development.</li></ul> 
2. Contribute to the Medical Plan
 
 
<ul><li>Develop territory Field Medical plan and TL Interaction plans based on therapeutic area objectives and TLs needs.</li></ul> 
<ul><li>Adopt institution/account planning approach and contribute to cross-functional institution/account plans.</li></ul> 
<ul><li>Contribute to development and delivery of scientifically meaningful medical programs/projects in line with the local Medical and Field Medical plan</li></ul> 
3. Provide Medical Support
 
 
<ul><li>As necessary and appropriate, support the initial and ongoing medical/scientific area and product specific training and provide key scientific updates to internal stakeholders (e.g. Commercial, Regulatory, Pharmacovigilance, Legal, HEOR, Market Access).</li></ul> 
<ul><li>Provide scientific support at promotional meetings by presenting unbiased scientific and clinical data, by evaluating speakers and by giving support to BMS-contracted speakers.</li></ul> 
4. Support Clinical Trial Activities
 
 
<ul><li>Support Interventional and Non-Interventional Research (NIR) studies (e.g. identification and assessment of potential study sites) to support patient recruitment and/or discussions around the safe and effective use of BMS investigational products, as agreed with local medical management and as defined by the study scope document.</li></ul> 
<ul><li>Provide recommendations and insights to clinical development team on study and site feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators, as agreed with local medical management.</li></ul> 
<ul><li>Actively support CRO sponsored studies as agreed with local medical management and as defined by the study scope document.</li></ul> 
<ul><li>Support HCPs in the ISR submission process as agreed with local medical management.</li></ul> 
5. Support Patient Safety Activities
 
 
<ul><li>Ensure that BMS Pharmacovigilance procedural documents are understood and applied by investigators of local studies, and alert appropriate BMS personnel to any identified Adverse Events.</li></ul> 

Degree Requirements 
 
<ul><li>Medical Doctor, Pharmacist</li></ul> 

Experience Requirements 
 
<ul><li>Working in a scientific and/or clinical research environment</li></ul> 
<ul><li>Translating scientific or clinical data into an understandable and valuable form to help physicians best serve their patients</li></ul> 
<ul><li>Developing peer-to-peer relationships with TLs and other healthcare professionals</li></ul> 

Key Competency Requirements 
 
<ul><li>Ability to work independently and act as a team player</li></ul> 
<ul><li>Good communication and presentation skills to present scientific and/or clinical data to research or healthcare professionals</li></ul> 
<ul><li>Ability to quickly and comprehensively learn about new subject areas</li></ul> 
<ul><li>Disease area knowledge and an understanding of scientific publications</li></ul> 
<ul><li>Experience in hematology, cardiology and/or oncology disease area is a plus</li></ul> 
<ul><li>Knowledge of a scientific or clinical area</li></ul> 
<ul><li>Knowledge of clinical trial design and process</li></ul> 
<ul><li>Knowledge of the national healthcare and access environment</li></ul> 
<ul><li>Knowledge of HEOR core concepts</li></ul> 
<ul><li>Excellent English language skills (speaking and writing)</li></ul> 

Travel Required 
 
<ul><li>Travel required (varies by geography)</li></ul> 

Other 
 
<ul><li>Located in Istanbul</li></ul> 
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
 
 
Uniquely Interesting Work, Life-changing Careers 
With a single vision as inspiring as Transforming patients' lives through science&trade; , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. 
 
On-site Protocol 
 
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
 
 
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
 
 
Supporting People with Disabilities 
 
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
 
 
Candidate Rights 
 
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
 
 
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
 
 
Data Protection 
 
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection . 
 
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. 
 
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
 
 
R1601009 : Medical Science Liaison</div>

Medical Science Liaison

Tandem Diabetes Care, Inc.

<div>GROW WITH US: 
Tandem Diabetes Care creates new possibilities for people living with diabetes, their loved ones, and their healthcare providers through a positively different experience. We&rsquo;d love for you to team up with us to &ldquo;innovate every day,&rdquo; put &ldquo;people first,&rdquo; and take the &ldquo;no-shortcuts&rdquo; approach that has propelled us to become a leader in the diabetes technology industry. 
STAY AWESOME: 
Tandem Diabetes Care is proud to manufacture and sell the Tandem Mobi system and t:slim X2 insulin pump with Control-IQ+ technology &mdash; an advanced predictive algorithm that automates insulin delivery. But we&rsquo;re so much more than that. Our company&rsquo;s human-centered approach to design, development, and support delivers innovative products and services for people who use insulin. Because many of our own team members live with diabetes, or have a loved one impacted by diabetes, the work is personal, and we are committed to the cause. Learn more at tandemdiabetes.com
A DAY IN THE LIFE:
The Medical Science Liaison (MSL) is a field-based scientific expert responsible for engaging with Key Opinion Leaders (KOLs), healthcare professionals, and medical practices to deliver evidence-based insights about the company&rsquo;s products and the latest scientific advancements. The MSL plays a pivotal role in translating clinical research into practical, real-world applications, ensuring that scientific knowledge is effectively communicated and utilized. In this role, the MSL actively contributes to educational programs, gathers valuable real-time insights from healthcare professionals (HCPs), and provides critical support to both internal and external stakeholders. Key responsibilities include representing the company at regional and national conferences, facilitating compliant scientific exchange, and engaging in appropriate off-label discussions with scientific peers, all while ensuring adherence to regulatory standards. This position is integral in bridging the gap between scientific innovation and clinical practice, driving informed decision-making within the medical community.
MSLs at Tandem are also responsible for the following in a specific region:
This role will cover the Central Region with our field team;
Ohio Valley to Wisconsin down to Gulf Coast areas.<ul><li>
Develops and executes Medical Affairs education strategies for the Central Area, delivering scientific webinars, in-person presentations, and fostering peer-to-peer scientific exchange.</li><li>
Partners closely with area-level commercial division leaders to engage healthcare professionals (HCPs) with peer-to-peer medical information exchange, relationship-building, and identification of appropriate fit for educational programs.</li><li>
Arranges in person travel opportunities to deliver scientific presentations and develop relationships with HCPs.</li><li>
Responds to both on-label and off-label inquiries from medical professionals on appropriate and safe device use and training, including virtual or in-person HCP consultations.</li><li>
Supports medical-marketing initiatives, such as conference planning and support, medical education content development, faculty speaker training, and review of promotional and educational materials.</li><li>
Supports Market Access teams with clinical presentations on publications, and market trends to payers and regulatory bodies.</li><li>
Provides ad-hoc educational webinars, presentations, or content to internal teams to support corporate initiatives (including scientific information, new indications for use, disease management, and device use).</li><li>
Assists with set up and delivery of round tables with peer HCPs to elicit feedback.</li><li>
Translates complex medical messages to enable clear and concise understanding by both external audiences and internal stakeholders.</li></ul>
WHAT YOU&rsquo;LL NEED:<ul><li>
MS, PhD, DNP, MD/DO, PharmD or equivalent combination of education and applicable job experience.</li><li>
Clinical licensure (MD, RN, NP, etc.) preferred.</li><li>
Certified Diabetes Care and Educator Specialist (CDCES), Board Certified in Advanced Diabetes Management (BC-ADM) or similar, preferred.</li><li>
3+ years of clinical diabetes, diabetes technology, or insulin pump industry experience.</li><li>
Experience presenting or communicating scientific information to professional audiences.</li><li>
Deep knowledge of diabetes disease state and clinical management of type 1 and type 2 diabetes, standards of care, and diabetes technology use in diverse populations.</li><li>
Fundamental knowledge and/or experience with scientific and statistical analyses.</li><li>
Professional experience interacting with patients, referral sources, and health care professionals.</li><li>
Skilled at analytical problem solving and communicating with culturally diverse groups. Skilled in effective presentations of scientific data and materials.</li><li>
Demonstrated knowledge of US FDA medical device regulations.</li><li>
Understanding of international medical device regulations with specific knowledge of Canadian Medical Device Regulations and EU CE Mark may be relevant.</li><li>
Excellent technical writing, editing, and proofreading skills.</li><li>
Able and motivated to work independently and as a team member with many different departments.</li><li>
Able to make and prioritize process and resource decisions based on overall team needs.</li><li>
Ability to plan and execute clinical and regulatory preparation activities.</li><li>
Skilled with MS Office applications as well as Adobe Acrobat.</li></ul>
TRAVEL:
Ability to travel by car or airplane (as well as overnights) independently up to 50% of the time and work a varied schedule to meet customer needs. Current negative Tuberculosis Skin Test and annual Tuberculosis screening with documented proof are required.
WHEN &amp; WHERE YOU&rsquo;LL WORK:
Remote: This position is remote and in the field, open to candidates within the United States. Equipment for the role will be provided and training will occur virtually.
COMPENSATION &amp; BENEFITS:
The starting base pay range for this position is $136,000 - $160,000 annually. Base pay will vary based on job-related knowledge, skills, experience and may also fluctuate depending on candidate&rsquo;s location and the overall job market. In addition to base pay, Tandem offers a competitive compensation package that includes bonus and a robust benefits package.
Tandem offers health care benefits such as medical, dental, vision available your first day, as well as health savings accounts and flexible saving accounts. You&rsquo;ll also receive 11 paid holidays per year, a minimum of 20 days of paid time off (with accrual starting on day 1) and you will have access to a 401k plan with company match as well as an Employee Stock Purchase plan. Learn more about Tandem&rsquo;s benefits here!
YOU SHOULD KNOW:
Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable state and local Fair Chance laws and regulations. A conditional offer of employment from Tandem is contingent upon successful completion of a pre-employment screening process comprised of a drug test (excluding marijuana) and background check, which includes a review of criminal history information.
Tandem has good cause to conduct a review of criminal history information of candidates for this position, as this role may involve access to proprietary, sensitive and/or confidential information, including customer protected health information. This review is required to ensure that individuals in such roles uphold high standards of trust and integrity so as to protect the interests of our customers, employees, and stakeholders.
SPONSORSHIP:
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
WHY YOU&rsquo;LL LOVE WORKING HERE: 
At Tandem, we believe joy fuels excellence. That's why we've built a workplace that celebrates your achievements and supports your well-being. Our team thrives on pushing boundaries and fostering growth, all while maintaining a spirit of fun and camaraderie. This is just one of the ways we stay awesome! Explore the benefits and reasons to love Tandem at https://www.tandemdiabetes.com/careers.
BE YOU, WITH US!
We embrace the value that every single one of us brings to the table. But sometimes we forget that when we don&rsquo;t meet 100% of a job description&rsquo;s criteria &ndash; maybe you&rsquo;re feeling that way right now? We encourage you to apply anyway. Because we want you to be you, with us.
Tandem is firmly committed to being an equal opportunity employer and does not discriminate on the basis of age, disability, sex, race, religion or belief, gender identity or expression, marriage/civil partnership, pregnancy/maternity, or sexual orientation. We are an inclusive organization, and we welcome applications from a wide range of candidates. Selection for roles will be based on individual merit alone.
REFERRALS: 
We love a good referral! If you know someone who would be a great fit for this position, please share!
APPLICATION DEADLINE:
 
The position will be posted until a final candidate is selected for the requisition or the requisition has a sufficient number of applications.
Make a move that matters. Join Tandem Diabetes Care, where we're turning challenges into triumphs every day and where your talents will help shape a healthier, happier tomorrow.
#LI-Remote #LI-DW1</div>

Medical Science Liaison - Central Region

<div>
 
 Job Title:
 
 
 CVRM
 
 
 Medical Scientific Liaison / Medical Advisor (Cairo / Giza)
 
 
 
 
 Introduction to role
 
 
 
 Here you&rsquo;ll have the opportunity to make a meaningful difference to patients&rsquo; lives. With science at its heart, this is the place where breakthroughs born in the lab become transformative medicines &ndash; for the world&rsquo;s most complex diseases. Answer unmet medical needs by pioneering the next wave of science, focusing on outcomes, and shaping the patient ecosystem. With our ground-breaking pipeline, the outlook is bright. Be proud to be part of a place that has achieved so much yet is still moving forward. There&rsquo;s no better time to join our global, growing enterprise as we lead the way for healthcare and society.
 
 
 
 Accountabilities
 
 
 
 <ul>
 <li>
 Medical Information Leadership: Deliver AstraZeneca&rsquo;s updated medical information to healthcare professionals across multiple channels, ensuring accuracy, relevance, and timely engagement that supports better clinical decisions.
 </li>
 <li>
 Clinical Study Management: Plan, initiate, and manage clinical studies to agreed quality, cost, and time standards; provide full monitoring services from start to finish to maintain scientific integrity and operational excellence.
 </li>
 <li>
 Project Delivery: Define scope, set milestones, and complete projects; provide clear, concise progress reports that drive alignment and enable swift, informed decisions.
 </li>
 <li>
 Team Development and Coaching: Share knowledge and coach colleagues to strengthen team capability, building consistent ways of working and elevating scientific standards.
 </li>
 <li>
 Patient Safety and Compliance: Ensure patient safety and uphold adverse event reporting standards in all interactions and activities, embedding compliance into daily practice.
 </li>
 <li>
 Named Patient Supply Governance: Manage the provision of named patient supplies in line with regulatory and ethical obligations, ensuring appropriate access and documentation.
 </li>
 <li>
 Pharmacovigilance Coordination: Coordinate pharmacovigilance systems to meet regulatory requirements and AstraZeneca standards, ensuring robust, timely safety oversight
 
 
 </li>
 </ul>
 
 Essential Skills/Experience
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s Degree in Pharma / Medical
 </li>
 <li>
 At least Three Years of experience in a multinational environment
 </li>
 <li>
 At least One Year of experience as MSL / Medical Advisor
 </li>
 <li>
 Fluency in spoken and written English language
 </li>
 <li>
 Cardiovascular / Renal / Metabolic Experience
 
 
 </li>
 </ul>
 
 Desirable Skills/Experience
 
 
 
 <ul>
 <li>
 Pharmaceutical experience is an asset
 </li>
 <li>
 Working towards MD/PHD
 </li>
 <li>
 Ability to interact and manage a range of stakeholders both internally and externally
 </li>
 <li>
 Knowledge of legislation relevant to Pharmaceutical Ecosystem
 </li>
 <li>
 Deep interest and understanding of science
 </li>
 <li>
 Strong collaborator and reflects strong influence capability
 </li>
 <li>
 Possess effective communication and facilitation skills
 
 
 </li>
 </ul>
 At AstraZeneca, we change the practice of medicine and improve the patient experience by generating and communicating compelling medical evidence. We translate our wealth of medical and scientific expertise to ensure that the data we produce helps physicians better treat patients at every point in their journey. Our culture is one of openness and transparency, fused with ambition and drive. We work seamlessly and inclusively across teams, roles, and levels to leverage our diverse skills and go further together. Join us in our mission to redefine cancer treatment and make a significant impact on patients' lives.
 
 
 
 Date Posted
 
 
 
 08-أبريل-2026
 
 
 
 Closing Date
 
 
 
 07-مايو-2026
 
 
 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
</div>

Medical Scientific Liaison / Medical Advisor (Cairo / Giza)

Swixx BioPharma

<div>
 
 
 Job Opportunity: Medical Science Liaison &ndash; Gulf
 
 
 
 
 
 
 
 Location
 
 :
 
 UAE / Kuwait
 
 
 
 
 
 
 
 About the Role:
 
 
 
 
 Medical Science Liaison (Rare Diseases) &ndash; Gulf
 
 position responsible for providing scientific and medical leadership across the Gulf region (UAE, Kuwait, Qatar, Oman, &amp; Bahrain) for Swixx and its partner companies. The person acts as the key medical expert, supporting strategy, clinical development, reimbursement, KOL engagement, and patient-focused initiatives while ensuring full compliance with national and EU regulations. It requires strong medical expertise, cross-functional collaboration, and the ability to communicate effectively with healthcare professionals, regulators, and internal teams to drive high-quality, ethical medical activities.
 
 
 
 
 
 
 Essential Requirements
 
 
 
 
 Education
 
 
 <ul>
 <li>
 BS in pharmacy or Doctor of Pharmacy (PharmD), provided that applicant has sufficient work experience in medical affairs in pharmaceutical or biotech industry or other stakeholders
 </li>
 </ul>
 
 
 
 
 
 Experience &amp; Knowledge
 
 
 <ul>
 <li>
 Not less than
 
 2 years&rsquo; experience
 
 in medical department as MSL or medical advisor in GCC
 </li>
 <li>
 Previous experience in
 
 rare diseases
 
 </li>
 <li>
 Previous experience in
 
 Cardiology, Neurology, Endocrinology, Genetic metabolic is a plus
 
 </li>
 <li>
 In-depth knowledge of the healthcare system combined with strong insight into customer needs
 </li>
 </ul>
 
 
 
 
 
 Skills and abilities
 
 
 <ul>
 <li>
 Familiarity with industry standards, codes and relevant legislation, including regulatory requirements and standards
 </li>
 <li>
 High level of professionalism, ability and willingness to work effectively with multiple products, projects and partners in cross-functional team setting
 </li>
 <li>
 Excellent communication (verbal and written), presentation, and interpersonal skills
 </li>
 <li>
 Fluent in official national language of the country (Arabic) and English
 </li>
 <li>
 Readiness for traveling on business purposes
 </li>
 </ul>
 
 
 
 
 
 Responsibilities
 
 
 
 As
 
 Medical Science Liaison
 
 you will be providing medical leadership and insights to the cross-functional teams. You will orchestrate high quality medical activities in adherence to internal and external requirements.
 
 
 
 
 
 <ul>
 <li>
 Support in developing and implementing country medical plan in the territory as agreed with Partners and in alignment with global medical strategy.
 </li>
 <li>
 Support Swixx and its Partners' medical activities and providing medical insight to marketing and business development.
 </li>
 <li>
 Support cross-functional teams to always ensure patient-focused activities, including timely responses to specific internal and external requests to discuss specific situations and challenges and provide medical affairs support to all stakeholders.
 </li>
 <li>
 Effective cooperation and communication with Swixx corporate functions and its Partners.
 </li>
 <li>
 Keep Swixx and its Partners' high reputation.
 </li>
 <li>
 Provide medical strategic recommendations for pipeline and life cycle management programs.
 </li>
 <li>
 Develops relationships with relevant medical groups (e.g. hospitals, professional associations, patient advocacy groups) in support of Swixx and its Partners' objectives.
 </li>
 <li>
 Planning, designing and managing medical advisory boards and gather insight from regional/national advisory boards; Supporting international advisory boards.
 </li>
 <li>
 Review and approval of promotional and non-promotional materials and activities.
 </li>
 <li>
 Acting as country medical information function, ensure timely response to medical information inquiries, processing and tracking of requests, quality check of related documentation
 </li>
 <li>
 Provide appropriate and timely medical support to commercial team, in line with local standards and regulations.
 </li>
 <li>
 Defining the country&rsquo;s medical resource needs and providing input for medical budget planning, resource allocation and budget management.
 </li>
 <li>
 Identifying training needs with other functional leaders and ensuring implementation of training programs.
 </li>
 </ul>
 
 
 
 
 
 Why Join Us?
 
 
 
 
 
 <ul>
 <li>
 Work &amp; learn in customer-oriented &amp; dynamic, fast-paced environment
 </li>
 <li>
 Have opportunity to contribute to impactful projects
 </li>
 <li>
 Be part of team driven by a cause
 </li>
 <li>
 Gain experience in multinational fast-growing company
 </li>
 </ul>
 
 
 
 
 If this opportunity excites you, we invite you to apply!
 
 
 
 
 
 Submit your application to careers.mena@swixxbiopharma.com not later than 19 April 2026.
 
 
 
 
 
 Only short-listed candidates will be contacted. All applications will be treated with strict confidentiality in compliance with GDPR regulations.
 
 
 
 
 
 Should you apply for the vacant position by sending your CV and other relevant information, you agree that Swixx Biopharma will process your personal data for its recruitment purposes. Swixx Biopharma will not keep your personal data for a period longer than required to perform the recruitment process for a specific vacant position, unless you explicit consent to keep your personal data in our database. We will not contact your previous or current employer without your explicit consent. More information about candidates&rsquo; personal data processing can be found in www.swixxbiopharma.com
 
 
 
 
 
 
 About Swixx Biopharma
 
 
 
 Swixx Biopharma is a trusted commercial platform for international companies seeking an indirect operating model. We collaborate with some of the world&rsquo;s most innovative pharmaceutical and biopharma companies to ensure patients have access to cutting-edge medicines, regardless of where they live. By providing a full suite of pharma services, we offer the expertise and capabilities of a multinational firm while maintaining a market-specific approach. For over a decade, our dedicated team is striving to make a meaningful impact on healthcare across Central and Eastern Europe, CIS/Eurasia, MENAT, and LATAM. Throughout our journey, our company has received numerous industry and business awards and is certified on several ISO standards.
 
 
 
 
 
 Swixx&rsquo;s recently published ESG strategy underscores our dedication to ethical business practices, environmental responsibility, and social impact. We are equally committed to upholding labor and human rights and fostering a diverse, inclusive, and equitable workplace, where every team member is valued and empowered to thrive.
 
</div>

Medical Science Liaison – Gulf

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