More jobs:
Senior Manager, Medical Affairs
Job in
Bridgewater, Plymouth County, Massachusetts, 02324, USA
Listed on 2026-08-30
Listing for:
Jobtailor
Full Time
position Listed on 2026-08-30
Job specializations:
-
Healthcare
Medical Science Liaison, Clinical Research -
Pharmaceutical
Medical Science Liaison
Job Description & How to Apply Below
- Support execution of Medical Affairs plans
- Translate Medical Affairs priorities into practical workplans, timelines, deliverables, and cross-functional follow-up
- Serve as a responsive medical point of contact for Commercial, Market Access, Regulatory, Legal, and field teams on assigned projects
- Coordinate assigned Medical Affairs activities across promotional review, field support, educational programs, insights, training and operational initiatives
- Participate in the development and maintenance of core scientific resources, including scientific narratives, internal medical updates, evidence summaries, and product or therapeutic area reference materials
- Serve as medical reviewer for promotional and non-promotional materials, ensuring scientific accuracy, fair balance, and alignment with approved labeling and substantiation
- Maintain organized medical review documentation, reference libraries, claims grids, and review-ready support materials
- Collaborate with Legal, Regulatory, Commercial, and external agencies to support review quality, reduce avoidable cycle-time delays, and maintain compliant ways of working
- Support field medical readiness through scientific content preparation, field training, insight collection, and follow-up on scientific engagement needs
- Participate in selected field engagements and external scientific meetings as appropriate to support compliant scientific exchange
- Participate in KOL, HCP, and stakeholder engagement planning support
- Assist with congress planning, advisory board preparation, medical booth support, scientific platform development, and speaker preparation in partnership with internal stakeholders and external vendors
- Coordinate development of audience-appropriate medical communications materials
- Ensure educational activities are scientifically balanced, compliant, and aligned with Medical Affairs strategy
- Track decisions, action items, timelines, and follow-ups from internal Medical Affairs meetings and assigned cross-functional initiatives to help ensure timely execution of priorities.
- Advanced scientific or clinical degree required (PharmD, PhD, MD, DO, NP or PA)
- 7+ years of experience within pharmaceutical, biotechnology, medical device, healthcare, clinical research, medical communications, or related environments
- Experience supporting Medical Affairs activities, scientific communications, MLR review, clinical development, regulatory affairs, or related functions
- Experience managing complex cross-functional projects and deliverables
- Ability to interpret clinical data, medical literature, product labeling, treatment guidelines, and scientific evidence
- Understanding of FDA-regulated pharmaceutical communications and compliant scientific exchange
- Excellent written and verbal communication skills
- Strong project management skills with ability to manage multiple priorities with an entrepreneurial mindset
- Ability to collaborate effectively across Medical Affairs, Commercial, Legal, Regulatory, Market Access, and external partners
- Strong attention to detail, scientific judgment, and execution discipline.
- Approximately 10-20% travel, including medical congresses, advisory boards, internal meetings, and other business activities.
Demonstrates expertise in Medical Affairs execution, scientific communication, and regulatory compliance, with a strong ability to manage cross-functional projects and deliverables. Proficient in interpreting clinical data and maintaining high standards of scientific accuracy in medical materials.
Highest-signal resume keywords- Advanced Scientific Degree
- Medical Affairs Experience
- Project Management Skills
- Regulatory Affairs Knowledge
- Scientific Communication
- Clinical Data Interpretation
- MLR Review
- Scientific Narrative Development
- Evidence Summary Creation
- Promotional Material Review
- Medical Communication Development
- Cross-Functional Project Management
- Regulatory Compliance
- Scientific Content Preparation
- Stakeholder Engagement
- Excellent Written Communication
- Excellent Verbal Communication
- Attention to Detail
- Execution Discipline
- Collaborative Mindset
- PharmD
- PhD
- MD
- DO
- NP
- PA
- Pharmaceutical
- Biotechnology
- Medical Device
- Healthcare
- Clinical Research
- Medical Communications
- FDA-Regulated Communications
- KOL Engagement
- HCP Engagement
- Medical Congresses
Position Requirements
10+ Years
work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×