Senior Manager, Medical Affairs

Cosette Pharmaceuticals, Inc.

Senior Manager in Medical Affairs at Cosette Pharmaceuticals managing medical projects and cross-functional collaboration. Supporting field engagements, scientific reviews, and educational initiatives in a dynamic environment.

Posted 7/14/2026full-timeBridgewater • New Jersey • 🇺🇸 United StatesSenior💰 $159,000 - $199,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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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 DegreeMedical Affairs ExperienceProject Management SkillsRegulatory Affairs KnowledgeScientific Communication

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data InterpretationMLR ReviewScientific Narrative DevelopmentEvidence Summary CreationPromotional Material ReviewMedical Communication DevelopmentCross-Functional Project ManagementRegulatory ComplianceScientific Content PreparationStakeholder Engagement

Soft Skills

Excellent Written CommunicationExcellent Verbal CommunicationAttention to DetailExecution DisciplineCollaborative Mindset

Certifications & Qualifications

PharmDPhDMDDONPPA

Industry Keywords

PharmaceuticalBiotechnologyMedical DeviceHealthcareClinical ResearchMedical CommunicationsFDA-Regulated CommunicationsKOL EngagementHCP EngagementMedical Congresses

About the role

Key responsibilities & impact

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

What you’ll need

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.

Benefits

Comp & perks

medical
dental
vision
life insurance
short-term disability
long-term disability
401(k) match
flexible spending accounts
health saving account
employee assistance program
tuition reimbursement program
parental leave
wellness program
paid time off
volunteer time
holidays