clinical science liaison

Sanofi

<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>
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Medical Science Liaison

<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>

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>

Dennis Jordanides, M.D., Inc.

About Us We are a boutique internal medicine concierge practice located in the heart of Newport Beach. We pride ourselves on delivering exceptional, personalized, and relationship-driven care to our patients. Our model is intentionally designed around a limited patient panel, allowing us to provide a thoughtful, elevated experience at every touchpoint.Role Overview As a Clinical Care Liaison, you serve as a vital connection between clinical care and the overall patient experience. This role combines strong back-office clinical skills with thoughtful coordination and communication, ensuring each patient interaction is seamless, attentive, and aligned with our standard of care.You will work closely with the physician and care team to support clinical workflows, coordinate services, and guide patients through their care with clarity and ease. A natural hospitality mindset and attention to detail are essential in this role.Responsibilities<ul><li>Greet and engage with patients in a warm, professional, and attentive manner</li><li>Support clinical operations, including rooming patients, obtaining vitals, and preparing for physician visits</li><li>Perform phlebotomy, EKGs, injections, and assist with in-office procedures as needed</li><li>Coordinate laboratory services, diagnostic imaging, and specialty referrals with a high level of follow-through</li><li>Serve as a clinical point of contact, helping patients navigate care plans and next steps</li><li>Communicate clearly with patients regarding instructions, results, and care coordination</li><li>Maintain accurate and timely documentation in the EMR</li><li>Ensure exam rooms, clinical supplies, and medications are organized and fully stocked</li><li>Uphold strict patient confidentiality and HIPAA compliance at all times</li><li>Collaborate closely with the front office and leadership team to ensure a seamless patient experience from start to finish</li><li>Anticipate patient needs and proactively address any barriers to care</li><li>Contribute to a positive, supportive, and high-performing team environment</li><li>Commit to personal and professional growth within the practice</li></ul>Qualifications<ul><li>Medical Assistant Diploma or Certification</li><li>Minimum of 3 years of clinical experience in a medical setting</li><li>Strong back-office experience required, including injections, vitals, and clinical workflows</li><li>Phlebotomy experience REQUIRED</li><li>Familiarity with EMR systems (Athena experience is a plus)</li><li>Solid understanding of HIPAA and patient privacy standards</li><li>Strong organizational skills with the ability to multitask and prioritize effectively</li><li>Clear, compassionate communication skills</li><li>Ability to work both independently and collaboratively within a small, high-touch team</li><li>REQUIRED: A hospitality-driven mindset, with a natural ability to create a warm, attentive, and elevated patient experience</li></ul>Why Join Us We are dedicated to creating an environment where both patients and team members feel genuinely cared for. This is an opportunity to be part of a practice that values clinical excellence, meaningful relationships, and a thoughtful, elevated approach to medicine.We look forward to welcoming a Clinical Care Liaison who shares our commitment to delivering exceptional care.Expected hours: 40.0 per weekExperience:<ul><li>Hospitality: 2 years (Required)</li><li>Phlebotomy: 3 years (Required)</li></ul>Language:<ul><li>English (Required)</li></ul>Ability to Commute:<ul><li>Newport Beach, CA 92663 (Required)</li></ul>Work Location: In person

Clinical Care Liaison

AstraZeneca

<div>Medical Advisor &ndash; Biologics 
 
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.
Join a high-performing team, empowered to cut through the noise and drive real change. Our agility and pace, coupled with scientific focus, powers us to spot opportunities in the market that keep us moving forward and into new spaces. 
 
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 pioneering the next generation of respiratory care, leveraging our deep heritage and a robust biologics pipeline to transform the lives of patients with chronic airway diseases. This high-impact therapy area addresses significant unmet medical needs in upper and lower airway conditions, including Asthma, COPD, Chronic Rhinosinusitis with Nasal Polyps (CRSwNP), and other future Indications.
The Medical Advisor, Biologics role ensures the delivery of high quality and impactful scientific engagement, medical education, evidence support, transform care and field insights generation in alignment with the respiratory and immunology TA priorities. The role is also responsible for driving the execution of medical activities and building advocacy with the relevant specialties across Saudi Arabia - Western Region in the assigned disease area.
You will act as a trusted partner to healthcare professionals, multidisciplinary centers of excellence, and cross-functional teams assuring that science, clinical precision, and patient outcomes remain at the core of every initiative.
This role requires strong therapeutic knowledge in biological therapies and airway diseases, scientific acumen, and the ability to connect field-based insights to the broader business and medical strategy during this critical phase of portfolio growth and new launches.
This role is responsible for a highly strategic product and disease area that involves working extensively with external stakeholders to forge strong relations and foster scientific and strategic partnerships within major hospitals and institutions/ authorities in their assigned territory and non-traditional stakeholders (E.g. policy and decision makers, payer groups, government, researchers, and others to help bridge the gaps and provide health system solutions.
What you&rsquo;ll do
Field Medical Excellence<ul><li>
Execute the Biologics Medical Affairs Plan in alignment with guidance from the TA Lead and cross-functional brand teams.</li><li>
Deliver scientific exchange with healthcare professionals (HCPs) and decision-makers to support the appropriate use of AstraZeneca&rsquo;s biologics portfolio.</li><li>
Drive the implementation of disease education, Multidisciplinary initiatives and patient identification projects for the current portfolio, while preparing the market for future indications.</li><li>
Support the rollout of launch readiness and lifecycle management activities for the assigned biologic therapies.</li></ul>
Scientific Engagement and External Collaboration<ul><li>
Build strong peer-to-peer relationships with Key External Experts (KEEs) of the targeted specialties within Saudi Arabia Western Region to advance disease area understanding, patient management and inform medical strategy.</li><li>
Organize, support, and present in scientific meetings, advisory boards, and symposia as a subject-matter expert in the assigned disease areas.</li><li>
Actively contributes to speaker training, CME partnerships, and scientific programs aligned with the biologics&rsquo; medical strategy.</li><li>
Gather and communicate actionable, scientific insights that inform the KSA local strategy and identify new opportunities for data generation or biologic access improvement.</li></ul>
Evidence Generation and Data Dissemination<ul><li>
Support the planning and operationalization of local studies, biologic registries, and Investigator-Initiated Studies (IIS) in coordination with the TA Lead, Evidence Generation, and Clinical Operations teams.</li><li>
Contribute to the development and review of scientific materials, ensuring accuracy, balance, and compliance with SFDA regulations.</li><li>
Disseminate emerging clinical data regarding biologic efficacy and safety to internal and external stakeholders in an ethical and scientifically objective manner.</li></ul>
Cross-Functional Medical Support<ul><li>
Partner closely with Market Access, Health Economics and Payer Evidence, Commercial, and Regulatory teams to ensure scientific and medical integrity in all activities across the KSA.</li><li>
Provide evidence-based medical input to hospital formularies, value communication, and payer interactions where appropriate.</li><li>
Deliver medical training and scientific support to internal colleagues (e.g., sales, market access, or respiratory specialty teams).</li></ul>
Compliance and Medical Governance<ul><li>
Ensure all activities comply with AstraZeneca ethical standards, SOPs, and Saudi Arabian local regulatory frameworks.</li><li>
Maintain up-to-date training on Ethical Interactions, GPEI, and any other Biologics-specific policies.</li><li>
Accurately document medical interactions, adverse event reports, and insights in compliance systems.</li></ul>
Essential for the role
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.
Essential Capabilities:<ul><li>
Bachelor&rsquo;s degree in medicine or pharmacy is required</li><li>
Post-graduate master&rsquo;s degree is an advantage</li><li>
2 or more years of experience in Medical Affairs roles, preferably within Respiratory and Immunology biologics.</li><li>
Experience supporting new launches.</li><li>
Proven ability to translate complex scientific data into clinical value for specialist physicians.</li><li>
Deep understanding of the Saudi Arabian healthcare system, including referral patterns, regulatory authority and access pathways.</li><li>
Excellence Communication, Influence, Planning and Organizational skills.</li><li>
Full understanding of the medical role in driving innovative value strategies, Health Economics &amp; Payer Evidence.</li><li>
Strategic and growth mindset with demonstrated business acumen.</li></ul>
Desirable Capabilities:<ul><li>
Experience supporting early-access programs and PSPs.</li><li>
Established track record of basic or clinical research.</li><li>
Active contribution to medical education or respiratory registry collaborations.</li><li>
Familiarity with real-world evidence (RWE), market access dossiers, or diagnostic collaborations.</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>

Medical Advisor– Biologics

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

General Dynamics Information Technology

<div><div><div>Your Impact
Own your opportunity to work alongside federal civilian agencies. Make an impact by providing services that help the government ensure the well being and support of U.S. citizens.
Job Description<div>
We are seeking a Scientific Computing Liaison to join a Scientific Technologies team supporting high-performance computing (HPC) and scientific research. This role serves as a critical bridge between researchers and HPC engineering staff, combining scientific domain knowledge with technical expertise to enable effective use of computational resources.
The ideal candidate will work closely with investigators to understand their scientific workflows, guide them in leveraging HPC resources, and collaborate with engineering teams to optimize performance and usability of the HPC environments.
This role is hybrid with 2-3 days a week onsite in Rockville, MD. Travel will not be reimbursed.
Responsibilities:
<ul><li>Serve as the primary liaison between scientific users and the HPC engineering team</li><li>
Engage with researchers to understand computational workflows, analysis pipelines, and scientific objectives</li><li>
Guide users in effectively leveraging HPC resources and adopting best practices</li><li>
Assist in troubleshooting scientific applications, pipelines, and data analysis workflows</li><li>
Translate scientific requirements into actionable input for HPC engineering improvements</li><li>
Identify opportunities to enhance user experience, documentation, and service offerings</li></ul>
WHAT YOU&rsquo;LL NEED TO SUCCEED:
Required qualifications:<ul><li>
Bachelor&rsquo;s degree in bioinformatics, computational biology, data science, or a related scientific field</li><li>
5+ years of hands-on experience with bioinformatics, scientific data analysis workflows, and/or related fields</li><li>
Familiarity with a variety of scientific software tools and analytical techniques</li><li>
Working knowledge of Unix/Linux-based environments and HPC systems (e.g., job schedulers, distributed computing)</li><li>
Experience in a customer-facing or service-oriented role supporting scientific users</li><li>
Ability to translate between scientific and technical audiences</li><li>
Ability to obtain and maintain a Public Trust</li></ul>
Desired skills and abilities:<ul><li>
Masters degree preferred</li><li>
Exposure to genomics, Cryo-EM data, or other large-scale biological datasets</li><li>
Familiarity with scripting languages such as Python, Bash, or R</li><li>
Experience optimizing or troubleshooting computational workflows</li><li>
Strong communication and problem-solving skills with a user-focused mindset</li><li>
Ability to manage multiple priorities and work effectively across teams</li><li>
Collaborative approach with a focus on enabling scientific outcomes</li></ul>
#GDITFedHealthJobs
</div></div><div><div><div>Work Requirements</div></div><div></div><div><div>
Years of Experience<div>
5 + years of related experience</div><ul><li>may vary based on technical training, certification(s), or degree</li></ul></div><div></div><div>
Certification</div><div>
Travel Required<div>
None</div></div></div></div></div><div>
Salary and Benefit Information<div>
The likely salary range for this position is $107,744 - $132,250. This is not, however, a guarantee of compensation or salary. Rather, salary will be set based on experience, geographic location and possibly contractual requirements and could fall outside of this range. 
View information about benefits and our total rewards program.</div>
About Our Work<div>
We are GDIT. A global technology and professional services company that delivers technology and mission services to every major agency across the U.S. government, defense and intelligence community. Our 30,000 experts extract the power of technology to create immediate value and deliver solutions at the edge of innovation. We operate across over 50 countries worldwide, offering leading capabilities in digital modernization, AI/ML, cloud, cyber and application development. Together with our customers, we strive to create a safer, smarter world by harnessing the power of deep expertise and advanced technology.</div><div>
Join our Talent Community to stay up to date on our career opportunities and events at gdit.com/tc.</div><div>
Equal Opportunity Employer / Individuals with Disabilities / Protected Veterans</div></div></div>

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