Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Encoded Therapeutics Inc.

Director, Medical Affairs

Encoded Therapeutics Inc.

. Define and implement the strategic plan for Encoded’s ETX301 clinical development program for pain .

Posted 10/3/2026full-timeRemote • United StatesLead💰 $225,000 - $310,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in clinical development and medical strategy, with a strong focus on building relationships with Key Opinion Leaders and managing complex projects in the pharmaceutical and biotech industries. Proficient in scientific communication, budget management, and compliance with industry regulations.

Highest-signal resume keywords
MD, PhD, Or MD/PhDClinical Development ExperienceNeuroscience ExpertiseStrong Presentation SkillsProject Management

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
Clinical Trial DesignInvestigator Sponsored StudiesEndpoint DevelopmentScientific CommunicationBudget ForecastingAnalytical SkillsRegulatory ComplianceGene Therapy ExperienceNeurologic Disease KnowledgeMedical Strategy
Soft Skills
CollaborationRelationship BuildingNegotiation SkillsTeamworkPrioritization
Industry Keywords
Pharmaceutical IndustryBiotech IndustryMedical AffairsKey Opinion LeadersAdvanced Therapy Medicinal ProductsPhase 1-3 ProgramsScientific PresentationsClinical ResearchMedical Exchange GuidelinesTravel Requirements

About the role

Key responsibilities & impact
  • Define and implement the strategic plan for Encoded’s ETX301 clinical development program for pain
  • Collaborate with Scientific Communications, Clinical Development, the Medical Office, and Patient Advocacy
  • Build relationships with Key Opinion Leaders to support clinical trial design and enrollment
  • Partner with Commercial, Strategy, Pre-clinical/Translational, Clinical Development/Operations, and Regulatory teams
  • Provide scientific and competitive insights from conferences and medical engagements
  • Develop and manage Investigator Sponsored Studies, observational studies, and other research supporting endpoint development or validation
  • Develop disease-state, mechanism-of-action, target-product-profile, and clinical-trial communication plans
  • Prepare or review scientific communication materials
  • Define and manage long-range budget forecasts
  • Identify, recruit, and manage vendors
  • Develop methods and procedures for scientific presentations
  • Represent Encoded and present data at advisory boards, investigator meetings, congresses, and other forums

Requirements

What you’ll need
  • MD, PhD, or MD/PhD in a relevant scientific or clinical discipline
  • For MD/MD-PhD: minimum of 4-6+ years of pharmaceutical/biotech industry experience in Medical Affairs, Clinical Development, or Medical Strategy
  • For a PhD: minimum of 5–8+ years of pharmaceutical/biotech industry experience with progressive leadership in Medical Affairs (MSL, Scientific Communications, Medical Strategy)
  • A minimum of 2–3 years specifically supporting clinical development of Phase 1–3 programs
  • Proven ability to develop internal relationships in a highly matrixed environment and external relationships with Key Opinion Leaders and industry experts
  • Prior experience and expertise in neuroscience and/or advanced therapy medicinal products (ATMPs)
  • Ability to lead by example, build interdependent partnerships, and foster collaboration and teamwork
  • Proven success in prioritization and management of several complex, concurrent projects with tight deadlines
  • Excellent written and verbal communication and high-level negotiation skills
  • Strong presentation skills
  • Strong analytical skills, especially understanding and interpreting scientific and clinical research and literature
  • Understanding of government and industry guidelines, regulations, and laws for scientific/medical exchange and communication
  • Travel up to 40%, including internationally, may be required
  • Gene therapy experience preferred
  • Neurologic disease experience, particularly pain programs or epilepsy, preferred
  • Experience across pre-clinical/clinical-stage and commercial-stage companies preferred

Benefits

Comp & perks
  • Comprehensive benefits package, including competitive employer premium contributions
  • Meaningful stock option grants
  • PTO, sick time and holiday pay
  • Generous Parental Leave program
  • Pre-tax medical and dependent care programs
  • STD, LTD, Life and AD&D
  • Professional development opportunities
  • Team-building events
  • Fully stocked micro - kitchen
  • Fitness center at South San Francisco location
  • Discretionary annual bonus
  • Discretionary stock-based long-term incentives