medical liaison

Avenues Recovery

<div>Who We Are
Avenues Recovery Center is a nationwide network of drug and alcohol rehab centers with eighteen locations across seven states. Offering the very highest standard of medical and clinical treatment, our services span every level of care - including detox, residential, PHP IOP, and outpatient services. Avenues is both JCAHO and CARF accredited, and in full compliance with all ASAM standards. Yet despite our excellence, our greatest strength remains the staff we cull from across the nation. If you're a compassionate professional who appreciates stimulating yet meaningful work, we warmly invite you to join our all-star team. 
Now hiring a Medical Liaison for our residential facility in South Bend, Indiana!
Hours: M-F 9am-5pm 
What You'll Do
The primary focus is to assist the medical personnel in the daily operations of the medical department.
Medical Care Protocols and Documentation
<ul><li>Schedule medical appointments with the providers upon admission and follow-ups
</li><li>Schedule external appointments for patients as assigned Coordinate with the BHT for patient transportation
</li><li>Obtain records from any external appointment and upload to electronic medical record (EMR)
</li><li>Documentation of all external appointments in EMR Utilize and maintain medical tracker on a daily basis
</li><li>Schedule labs as ordered
</li><li>Maintain patient records in EMR, including but not limited to, uploading PDMP
</li><li>Clear orders from eRx for discharged patients
</li><li>Ensure pharmacy orders and prescription authorizations are completed
</li><li>Review rejected prior authorizations and document appropriately
</li><li>Perform other duties as assigned.
</li></ul>Coordination of Care
<ul><li>Obtain and process all pharmacy authorizations, pending refills
</li><li>Obtain prior authorization for Sublocade and Vivitrol injections
</li><li>Schedule MAT injections and communicate with the nursing staff
</li><li>Ensure pharmacy delivers based on facility set-up
</li><li>Communicate with the pharmacy on any issues
</li><li>Communication and collaboration with treatment team is critical
</li><li>Notify appropriate staff of all patient concerns
</li><li>Managing supplies needed for medical department.
</li><li>Follow up and accountability for medication issues</li></ul> 
What We're Looking For<ul><li>
High school diploma</li><li>
QMA license in IN preferred</li><li>
Experience in substance use disorder (SUD) and/or behavioral health settings strongly preferred, with demonstrated understanding of recovery-oriented care and patient-centered support.</li></ul> 
Why Join Us
Avenues features a rich, fulfilling workplace culture where every person is valued and greatness is pursued. We support our employees unconditionally, and work to provide them with every resource they need to excel! Aside from generous PTO and compensation, when you join the Avenues family, you'll be eligible for the following benefits package:<ul><li>
401K with employer match</li><li>
Medical Insurance
</li><li>Dental
</li><li>Vision</li><li>
Accident</li><li>
Critical Illness</li><li>
Hospital Indemnity</li><li>
Voluntary Short-Term Disability</li><li>
Voluntary Long -Term Disability</li><li>
Employer-Paid Life and AD&amp;D</li><li>
LifeTime Benefit Term Insurance with Long Term Care</li><li>
Legal Coverage</li><li>
Pet Insurance</li><li>
Identity Theft Protection</li><li>
Employer-Paid Employee Assistance Program</li><li>
Flexible Spending Account (FSA) - Medical</li><li>
Dependent Care FSA (DCF)</li></ul> 
Join our growing team and discover the magic here at Avenues! 
Apply today!</div>

Medical Liaison

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

Sanofi

<div>Job title: Medical Science Liaison &ndash; Immunology (Respiratory &amp; GI)<ul><li>
Location: Jeddah, Kingdom of Saudi Arabia
</li></ul>About the job
As a Medical Science Liaison &ndash; Immunology (Respiratory &amp; GI) within our Specialty Care team, you'll serve as the vital bridge between cutting-edge science and clinical practice. You'll build trusted relationships with key scientific experts, support clinical research initiatives, and bring real-world medical insights back to our brand teams to help shape breakthrough treatments for patients with immune challenges. Ready to get started?
Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you'll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.
About Sanofi
We're an R&amp;D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.
Main responsibilities<ul><li>
Build and maintain balanced scientific relationships with key external experts to deepen understanding of customer research needs and opportunities in Immunology (Respiratory &amp; GI).</li><li>
Develop a clear understanding of the healthcare ecosystem through stakeholder mapping and identifying key milestones in patient journeys.</li><li>
Provide healthcare professionals and decision-makers with accurate, balanced, and timely scientific information about our Immunology portfolio.</li><li>
Collaborate closely with Medical Affairs and clinical teams to coordinate Phase IV clinical projects, facilitate investigator-sponsored study submissions, support publications, and assist in site selection.</li><li>
Act as a product expert supporting commercial teams during training sessions, particularly in handling medical objections.</li><li>
Serve as the primary source of real-world medical insights and scientific expert feedback from the field to brand teams.</li><li>
Represent Sanofi at key medical and scientific conferences by staffing medical information booths, gathering competitive intelligence, and observing sponsored speakers.</li><li>
Receive, document, and report adverse events according to company procedures and ensure risk management plan implementation and monitoring.</li></ul>
About you<ul><li>
Education: University degree in life sciences required; MD, PhD, or PharmD strongly preferred</li><li>
Experience: At least 2 years of experience in specialty care and/or Immunology/Gastroenterology is a plus</li><li>
Technical skills: Strong knowledge of clinical research methodology and Good Clinical Practice (GCP)</li><li>
Communication skills: Ability to communicate effectively at various management levels, including with scientific external experts</li><li>
Soft skills: Self-motivated team player with business acumen, resource planning abilities, and the capacity to inspire and motivate others</li><li>
Languages: Full professional proficiency in English and Arabic</li></ul>
Why choose us?<ul><li>
Work at the intersection of cutting-edge immunoscience and patient care, helping deliver breakthrough treatments to those with the highest unmet medical needs.</li><li>
Build meaningful relationships with leading scientific experts and key opinion leaders while contributing to clinical research that shapes the future of Immunology care.</li><li>
Develop your career in a purpose-driven environment with opportunities to grow across therapeutic areas, functions, and geographies.</li><li>
Collaborate with diverse, multidisciplinary teams across Medical Affairs, Clinical Research, and Commercial functions to drive patient impact.</li><li>
Thrive in a workplace that values scientific excellence, ethical leadership, and your personal well-being with comprehensive benefits and flexible working options.</li></ul>
Pursue Progress. Discover Extraordinary.
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what's never-been-done-before. You'll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people's lives? Let's Pursue Progress and Discover Extraordinary &ndash; together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law
null</div>

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

<div><div><div><div>Job title: Medical Science Liaison &ndash; Immunology (Respiratory &amp; GI)<ul><li>
Location: Riyadh, Kingdom of Saudi Arabia</li></ul>
About the job
As a Medical Science Liaison &ndash; Immunology (Respiratory &amp; GI) within our Specialty Care team, you'll serve as the vital bridge between cutting-edge science and clinical practice. You'll build trusted relationships with key scientific experts, support clinical research initiatives, and bring real-world medical insights back to our brand teams to help shape breakthrough treatments for patients with immune challenges. Ready to get started?
Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you'll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.
About Sanofi
We're an R&amp;D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.
Main responsibilities<ul><li>
Build and maintain balanced scientific relationships with key external experts to deepen understanding of customer research needs and opportunities in Immunology (Respiratory &amp; GI).</li><li>
Develop a clear understanding of the healthcare ecosystem through stakeholder mapping and identifying key milestones in patient journeys.</li><li>
Provide healthcare professionals and decision-makers with accurate, balanced, and timely scientific information about our Immunology portfolio.</li><li>
Collaborate closely with Medical Affairs and clinical teams to coordinate Phase IV clinical projects, facilitate investigator-sponsored study submissions, support publications, and assist in site selection.</li><li>
Act as a product expert supporting commercial teams during training sessions, particularly in handling medical objections.</li><li>
Serve as the primary source of real-world medical insights and scientific expert feedback from the field to brand teams.</li><li>
Represent Sanofi at key medical and scientific conferences by staffing medical information booths, gathering competitive intelligence, and observing sponsored speakers.</li><li>
Receive, document, and report adverse events according to company procedures and ensure risk management plan implementation and monitoring.</li></ul>
About you<ul><li>
Education: University degree in life sciences required; MD, PhD, or PharmD strongly preferred</li><li>
Experience: At least 2 years of experience in specialty care and/or Immunology/Gastroenterology is a plus</li><li>
Technical skills: Strong knowledge of clinical research methodology and Good Clinical Practice (GCP)</li><li>
Communication skills: Ability to communicate effectively at various management levels, including with scientific external experts</li><li>
Soft skills: Self-motivated team player with business acumen, resource planning abilities, and the capacity to inspire and motivate others</li><li>
Languages: Full professional proficiency in English and Arabic</li></ul>
Why choose us?<ul><li>
Work at the intersection of cutting-edge immunoscience and patient care, helping deliver breakthrough treatments to those with the highest unmet medical needs.</li><li>
Build meaningful relationships with leading scientific experts and key opinion leaders while contributing to clinical research that shapes the future of Immunology care.</li><li>
Develop your career in a purpose-driven environment with opportunities to grow across therapeutic areas, functions, and geographies.</li><li>
Collaborate with diverse, multidisciplinary teams across Medical Affairs, Clinical Research, and Commercial functions to drive patient impact.</li><li>
Thrive in a workplace that values scientific excellence, ethical leadership, and your personal well-being with comprehensive benefits and flexible working options.</li></ul>
Pursue Progress. Discover Extraordinary.
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what's never-been-done-before. You'll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people's lives? Let's Pursue Progress and Discover Extraordinary &ndash; together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law</div></div></div>
null</div>

AstraZeneca

<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)

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

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