Director, Medical Affairs

As Director of Medical Affairs, you are a senior scientific leader within Click Therapeutics' Medical Affairs organization, working across our portfolio. Reporting to the Vice President of Medical Affairs, you own the scientific evidence and the scientific relationships that establish our treatments with clinicians, payers and the wider medical community: what the evidence says, what it means clinically and economically, where the gaps are, and how it reaches the people who make treatment and coverage decisions.

Responsibilities

Define the medical strategy for each asset, including the target patient profile, clinical place in therapy, and the priorities that guide evidence generation and scientific engagement; Establish the clinical meaningfulness of trial endpoints and outcome measures, and monitor the clinical and competitive landscape to identify emerging tactics, arguments and gaps in our data packages; Own the evidence plan to address the evidence needs of clinicians and payers, and drive its execution; Develop and maintain the Core Medical Narrative for each asset, and build the field medical materials, medical value story decks and payer-facing scientific content, including the clinical sections of Value Dossiers and evidence packages with Market Access; Own the publication and congress plan, managing medical communications agencies and writers as the scientific reviewer accountable for accuracy and balance; Establish and own Medical Information to support timely, accurate and balanced responses to unsolicited requests from HCPs; Own the engagement strategy for each asset: identify, segment and prioritize the national and regional experts, institutions and payer clinical decision-makers; Lead compliant peer-to-peer scientific exchange with clinical experts, health systems, advocacy organizations and payer medical leadership, and direct our scientific presence at major congresses and advisory boards; Drive and synthesize field insight into recommendations that shape medical strategy, scientific content and evidence priorities

Requirements

Advanced degree required (MD, DO, PhD or PharmD); 10+ years of combined industry, academic, clinical research, or other clinical practice experience, of which at least 5 years in the pharmaceutical industry, including experience supporting a product launch; Demonstrated experience building medical value stories, scientific narratives and medical response content that hold up with clinicians, payers and regulators; Experience planning and executing evidence and publication strategy, including study design, protocol development and CRO, agency and vendor management; Prior field-based experience, such as an MSL role, with a track record of building peer-to-peer scientific relationships with clinical experts and payer decision-makers and translating those conversations into medical impact; Strong analytical judgment: able to interpret trial statistics and outcome measures; critically assess evidence strengths and gaps; and communicate complex data clearly

Nice to have

Knowledge of or experience with Digital Therapeutics and/or Prescription Digital Therapeutics; Experience establishing Medical Affairs infrastructure in an early-stage or pre-commercial organization

Benefits

Competitive Salary with Annual Review; Cash Bonus; Stock Options; 5% 401(k) matching; Medical; Dental; Vision; Life Insurance; Voluntary Benefits; Unlimited PTO; Uber One; Nectar Rewards; One Medical; Fitness Reimbursement; Bike Membership; Professional Development Stipend; DoorDash; Parent Benefits; LinkedIn Learning; Gemini Enterprise Stack; Claude; Industrious Workspaces; Commuter Subsidies; Flexible Work Arrangement; Sponsored Company Events; Office Snacks and Beverages