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About the Role

As Director of Medical Affairs, you are a senior scientific leader within Click Therapeutics' Medical Affairs organization, working across our portfolio. You will own the scientific evidence and relationships that establish our treatments with clinicians, payers, and the medical community. This role involves building medical strategy and tactics, developing evidence strategy and medical materials, engaging experts, directing agencies, and establishing Medical Information and governance.

Responsibilities

Define the medical strategy for each asset, including target patient profile, clinical place in therapy, and priorities for evidence generation and scientific engagement.
Establish the clinical meaningfulness of trial endpoints and outcome measures.
Monitor the clinical and competitive landscape to identify emerging tactics, arguments, and data gaps.
Own and execute the evidence plan to address clinician and payer needs.
Develop and maintain the Core Medical Narrative for each asset.
Build field medical materials, medical value story decks, and payer-facing scientific content.
Own the publication and congress plan, managing medical communications agencies and writers.
Establish and own Medical Information to provide accurate responses to unsolicited requests from HCPs.
Own the engagement strategy for each asset, identifying and prioritizing key experts, institutions, and payer decision-makers.
Lead compliant scientific exchange with clinical experts, health systems, advocacy organizations, and payer medical leadership.
Direct scientific presence at major congresses and advisory boards.
Synthesize field insights into recommendations for medical strategy, scientific content, and evidence priorities.

Requirements

Seamlessly integrated AI into professional workflow and personal productivity.
Advanced degree required (MD, DO, PhD or PharmD).
10+ years of combined industry, academic, clinical research, or other clinical practice experience.
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.
Experience planning and executing evidence and publication strategy, including study design, protocol development, and CRO, agency, and vendor management.
Prior field-based experience (e.g., MSL role) with a track record of building peer-to-peer scientific relationships.
Strong analytical judgment to interpret trial statistics and outcome measures.
Ability to critically assess evidence strengths and gaps.
Ability to communicate complex data clearly.
Knowledge of or experience with Digital Therapeutics and/or Prescription Digital Therapeutics is considered a plus.
Experience establishing Medical Affairs infrastructure in an early-stage or pre-commercial organization.

Skills

AI integration
Medical strategy
Evidence generation
Scientific engagement
Clinical meaningfulness
Data analysis
Publication planning
Scientific communication
External engagement
Scientific exchange
Analytical judgment

Location

Tribeca, NYC
Remote

Work Type

Hybrid

Experience Level

10+ years of experience
5+ years in pharmaceutical industry

Education Level

Advanced degree (MD, DO, PhD or PharmD)

Salary/Compensations

$175,000 - $220,000 base salary
Annual performance-based cash bonus
Generous equity package

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

About the Company

Develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs.
Leading innovator of Digital Therapeutics™, delivering accessible, clinically proven, FDA-regulated prescription treatments.
Treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design.
Achieves compelling clinical outcomes for patients seeking new treatment options.
Continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning.
Digital therapeutics address diverse therapeutic needs including psychiatry, neurology, oncology, immunology, and cardiometabolic diseases.
Consistently named a best place to work.
Fosters an inclusive, diverse workforce united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics.
Fast-growing pre-IPO company in a nascent and fast-growing space.

Equal Opportunity

Committed to equal opportunity in employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status.
Complies with all applicable national, state and local laws governing nondiscrimination in employment.
Complies with employment eligibility verification requirements of the Immigration and Nationality Act.
All applicants must have authorization to work for Click Therapeutics in the U.S.
May support applications for temporary visa classification and/or sponsor applications for permanent residence.
Employment applicants requiring immigration sponsorship must disclose authorization to work in the U.S. at the time of initial application.