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Senior Manager, Medical Affairs

Job in Bridgewater, Plymouth County, Massachusetts, 02324, USA
Listing for: Jobtailor
Full Time position
Listed on 2026-08-30
Job specializations:
  • Healthcare
    Medical Science Liaison, Clinical Research
  • Pharmaceutical
    Medical Science Liaison
Salary/Wage Range or Industry Benchmark: 120000 - 150000 USD Yearly USD 120000.00 150000.00 YEAR
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.
Requirements
  • 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.
Core Competencies

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
ATS Optimization Keywords Hard Skills
  • 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
Soft Skills
  • Excellent Written Communication
  • Excellent Verbal Communication
  • Attention to Detail
  • Execution Discipline
  • Collaborative Mindset
Certifications & Qualifications
  • PharmD
  • PhD
  • MD
  • DO
  • NP
  • PA
Industry Keywords
  • Pharmaceutical
  • Biotechnology
  • Medical Device
  • Healthcare
  • Clinical Research
  • Medical Communications
  • FDA-Regulated Communications
  • KOL Engagement
  • HCP Engagement
  • Medical Congresses
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Position Requirements
10+ Years work experience
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