Senior Director – Global Medical Affairs, Evidence Generation

Scholar Rock

. Lead development and execution of global evidence generation strategies supporting product value demonstration, reimbursement, market access, and lifecycle management .

Posted 11/2/2026full-timeCambridge • Massachusetts • United StatesSenior💰 $200,000 - $325,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in leading global evidence generation strategies, managing complex projects, and fostering collaboration across cross-functional teams within the pharmaceutical and biotechnology sectors. Proven ability to establish relationships with key stakeholders and deliver measurable outcomes in real-world evidence and outcomes research.

Highest-signal resume keywords

Evidence GenerationReal-World EvidenceOutcomes ResearchProject ManagementCross-Functional Collaboration

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Observational StudiesDatabase AnalysisPatient-Reported Outcome ResearchPhase IV StudiesPost-Hoc AnalysesPublication Strategy DevelopmentKPI ManagementBudget ManagementVendor Relationship ManagementScientific Rigor

Soft Skills

Strong Communication SkillsExceptional Interpersonal CapabilitiesCollaborationInnovationPatient Focus

Certifications & Qualifications

MDPhDPharmD

Industry Keywords

Pharmaceutical IndustryBiotechnology IndustryLife SciencesNeuromuscular DiseasesRare DiseasesHealth Technology AssessmentMarket AccessMedical Affairs

About the role

Key responsibilities & impact

Lead development and execution of global evidence generation strategies supporting product value demonstration, reimbursement, market access, and lifecycle management
Direct design, implementation, and operational oversight of Medical Affairs-led evidence generation initiatives
Oversee prospective and retrospective observational studies, real-world evidence studies and database analyses, patient-reported outcome research, qualitative and quantitative primary research, Phase IV studies, and post-hoc analyses
Partner with cross-functional teams to integrate evidence generation into commercial evaluations and portfolio management decisions
Establish and maintain relationships with key opinion leaders, clinical researchers, healthcare decision-makers, payers, HTA bodies, health systems, and advocacy organizations
Develop publication and dissemination strategies with Medical Communications
Support development and training of global and regional Medical Affairs teams
Manage multiple evidence generation projects, KPIs, budgets, CROs/vendors, and external collaborations
Foster scientific rigor, innovation, compliance, collaboration, and patient focus
Report to the VP, Global Medical Affairs

Requirements

What you’ll need

MD, PhD, PharmD, or equivalent advanced degree in a relevant life sciences discipline
Director level: Minimum 3–5 years of experience in Evidence Generation, Real-World Evidence, Outcomes Research, or related functions within the pharmaceutical, biotechnology, or life science industry
Senior Director level: Minimum 6–8+ years of experience in tracking, design, and executive delivery of complex global evidence generation strategies within the biopharmaceutical industry
Documented track record of delivering measurable project results and cross-functional success
Strong written and verbal communication skills
Exceptional interpersonal capabilities
Proven experience managing external vendor relationships
Prior experience in neuromuscular diseases and/or rare diseases highly preferred but not required
Ability to travel domestically and internationally (~15%)

Benefits

Comp & perks

Equal Opportunity Employer committed to diversity and inclusion
Hybrid work arrangement
Approximately 15% domestic and international travel