medical scientific liaison

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)

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)

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>
null</div>

Medical Science 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>

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>

Scientific Computing 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
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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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