Viridian Therapeutics

Senior Director, Medical Director

Viridian Therapeutics • $180K — $220K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • MD degree required with over 15 years of relevant experience
  • 5+ years of experience in the pharmaceutical or biotech industry
  • Preferred therapeutic area experience in ophthalmology or endocrinology
  • Strong understanding of industry regulations and guidelines
  • Proficient in scientific communication strategies and KOL insights
  • Strong analytical and organizational skills with attention to detail
  • Excellent interpersonal skills for stakeholder relationship management

Responsibilities

  • Develop and lead US Medical Affairs strategy across all phases of product lifecycle
  • Translate complex clinical data into clear medical narratives
  • Represent Medical Affairs in cross-functional governance forums
  • Provide clinical review for Medical Information to ensure scientific accuracy
  • Serve as the primary medical reviewer for promotional materials
  • Support field medical teams with clinical leadership and KOL interactions
  • Oversee investigator sponsored research (ISR) and Phase 4 studies

Benefits

  • Competitive pay and stock options
  • Comprehensive medical, dental, and vision coverage
  • Fertility and mental health support programs
  • Disability coverage
  • 401(k) with company match and immediate vesting
  • Generous vacation and holiday shutdowns
  • Employee Stock Purchase plan
  • Coverage for various mental and physical health programs
Full Job Description
Description

Reporting to the Head of Medical Affairs, the Senior Director, Medical Affairs will partner with key colleagues to develop, lead, and execute medical strategies aligned with the broader organization while providing progress updates to relevant stakeholders. This individual will help ensure our medical strategy is clinically meaningful, scientifically rigorous and shape evidence generation, scientific communications, and external engagement across the lifecycle of our therapies-from early pipeline through launch and post-approval.

This role may be based in our Waltham, MA headquarters, which would be a hybrid role, or it can also be fully remote. Our office-based employees are required to work in the office three (3) days a week. If remote, travel to headquarters for meetings would be required at the discretion of management.

Responsibilities (including, but not limited to):

Medical Strategy & Leadership
  • Provide physician led strategic direction for the US Medical Affairs strategy across pre-launch, launch, and post-launch phases
  • Translate complex clinical and scientific data into clear, credible medical narratives to support scientific exchange, education, and evidence-based decision-making
  • Represent US Medical Affairs on cross-functional governance bodies and strategic forums

Internal Medical Leadership
  • Provide clinical review and guidance for Medical Information content to ensure scientific accuracy, appropriate clinical interpretation, and compliance with regulations/policies.
  • Serve as the primary medical reviewer for US promotional materials, ensuring scientific integrity, clinical relevance, fair balance, and compliance with regulations, policies, and standards.
  • Apply medical judgment throughout the review process in partnership with Commercial, Regulatory, and Legal stakeholders

Field Medical Affairs & External Engagement
  • Provide clinical leadership and scientific guidance to support field medical needs, including MSL training, scientific readiness, and participation in KOL interactions
  • Depending on compound, lead and/or participate in advisory boards, investigator meetings, and scientific exchange activities in a compliant, non-promotional manner

Lead and oversee US medical research efforts
  • Oversight of investigator sponsored research (ISR) and leading Phase 4 studies, from strategic planning to data readout
  • Ensure studies address meaningful clinical and scientific questions, generate high-quality data, and align with overall medical and evidence-generation strategy

Pipeline & Early-Stage Assets
  • Act as the Medical Affairs lead for early-stage pipeline programs (FcRn and TSHR asset)
  • Provide medical input into development strategy, target product profiles, evidence needs, and external scientific positioning in close collaboration with cross-functional partners.


Requirements

  • MD required with 15+ years of relevant work experience with 5+ years in pharma/biotech industry; therapeutic area experience in ophthalmology or endocrinology preferred.
  • Strong knowledge of relevant industry rules and guidelines
  • Prior experience and in-depth knowledge of effective strategies in scientific communications/ publications and KOL insights highly desired
  • Ability to critically analyze and summarize scientific data
  • Proven planning and organizational skills with experience managing multiple priorities; anticipation and attention to detail with the ability to prioritize
  • Strong interpersonal skills in developing and maintaining professional relationships with internal and external stakeholders
  • Strong consulting, facilitation, and communication skills bridging between scientific and business priorities to manage effective and solid working collaboration cross-functionally
  • Ability to travel as required to support scientific communications efforts
  • Strong commitment to ethical standards
  • Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
  • Ability to travel up to 25-40%
  • The salary range for this position is commensurate with experience


Viridian offers a comprehensive benefits package including:
  • Competitive pay and stock options for all employees
  • Competitive Medical, dental, and vision coverage
  • Fertility and mental health programs
  • Short- and long-term disability coverage
  • Life, Travel and AD&D
  • 401(k) Company Match with immediate company vest
  • Employee Stock Purchase plan
  • Generous vacation plan and paid company holiday shutdowns
  • Various mental, financial, and proactive physical health programs covered by Viridian


About Viridian Therapeutics

Viridian Therapeutics is a biotechnology company that develops gene therapies for inherited diseases. The company's lead product candidate, VRDN-001, is a gene therapy for Friedreich's ataxia, a rare genetic disease that causes progressive damage to the nervous system. Viridian Therapeutics was founded in 2018 and is headquartered in Cambridge, Massachusetts.
Learn more about Viridian Therapeutics
Size
10 employees
Market Cap
$1.1 billion
Industry
Net Income
-$30 million
5 Year Trend
-3.1%
Revenue
$1.8 million
NASDAQ

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