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About the Role

The Director / Senior Director, Science plays an integral role that bridges scientific innovation, product development, clinical evidence, and commercial strategy. This person will act as a key scientific representative for Click, driving scientific communications and heavily enabling Business Development efforts. Because we operate in a lean, fast-paced environment, the ideal candidate is highly flexible, action-oriented, and not overly process-driven. You will act as a scientific subject matter expert who can seamlessly pivot to support various products across our pipeline. We are looking for an MD or PhD with a strong academic and publication record who is eager to write, speak, and publish externally to elevate Click’s scientific presence, while actively driving business partnerships forward.

Responsibilities

Take a leading role in writing and publishing peer-reviewed papers, white papers, and clinical data presentations.
Actively represent Click at external scientific, medical, and industry conferences.
Identify, build and maintain relationships with Key Opinion Leaders (KOLs), clinicians, and academic researchers.
Translate complex clinical data and evidence-based medicine into compelling scientific narratives for external audiences, ensuring actionable insights are communicated effectively.
Provide deep scientific and medical credibility to business development efforts.
Partner closely with the commercial and BD teams to evaluate opportunities, conduct scientific diligence, and create compelling proposals for partners.
Serve as a scientific face of the company for existing and emerging partnerships, acting as a liaison between external stakeholders and internal R&D/product teams.
Operate comfortably in a lean, dynamic startup environment.
Provide hands-on scientific and medical leadership across multiple digital therapeutic products and pipeline assets as needed on a day-to-day basis.
Work closely with product, clinical, and regulatory teams to ensure that product development aligns with the latest clinical evidence and market access requirements in a regulated space.

Requirements

A doctoral/professional degree (MD, PhD, PsyD, PharmD) is required.
Deep expertise in a CNS discipline (e.g., psychiatry, neurology, psychology) and experience with evidence-based nonpharmacological / biobehavioral treatment is required.
Experience in migraine or headache disorders, as well as wearable data, is highly preferred.
Clinical practice experience is a plus.
5+ years of experience in the life sciences, digital health, or pharmaceutical industry within a regulated space.
Prior experience in product development, Medical Affairs, Scientific Affairs, or Commercial/BD enablement is highly desired.
Established record and proven willingness to write, publish, and speak externally.
Highly flexible, adaptable, and action-oriented.
Not overly process-driven; able to thrive in a fast-paced environment and roll up your sleeves to support various products and initiatives simultaneously.
Exceptional ability to translate complex scientific and clinical concepts into business opportunities and accessible language for diverse audiences.
AI is a present-day prerequisite; seamlessly integrate AI into professional workflow and personal productivity.

Skills

Scientific Communications
External Leadership
Stakeholder Engagement
Business Development Enablement
Strategic Growth
Product Collaboration
AI Integration

Location

Tribeca, NYC
Boston, MA

Work Type

Hybrid

Experience Level

Director
Senior Director
5+ years

Education Level

MD
PhD
PsyD
PharmD

Salary/Compensations

$165,000 - $195,000

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
Fertility Support
Fitness Reimbursement
Bike Membership
Professional Development Stipend
DoorDash and Catered Lunches
Parent Benefits
LinkedIn Learning
Gemini Enterprise Stack
Industrious Workspaces
Commuter Subsidies
Flexible Work Arrangement
Choice of Mac or Windows
Sponsored Company Events
Office Snacks and Beverages

About the Company

Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs.
As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand.
Click’s treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process.
This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options.
Click Therapeutics 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.
The digital therapeutics under development on Click’s platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases.
Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics.
For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn.

Equal Opportunity

Click Therapeutics is committed to equal opportunity in the terms and conditions of 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.
Click Therapeutics also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act.
All applicants must have authorization to work for Click Therapeutics in the U.S.
In certain circumstances it may be advantageous to Click Therapeutics to support the application(s) for temporary visa classification and/or sponsor applications for permanent residence so that a foreign national colleague can accept or remain in a work assignment in the U. S.
For certain classes of temporary visas, the resulting work authorization may be specific to Click Therapeutics and the specific job and/or work site.
Click Therapeutics may at its business discretion decide to or refrain from obtaining, maintaining and/or extending the temporary visa status and/or sponsoring a colleague for permanent residency and /or employment eligibility, considering factors such as availability of qualified U.S. workers and the colleague's long-term prospects for securing lawful permanent residence, among other reasons.
Employment applicants requiring immigration sponsorship must disclose, when initial application for employment is made, whether or not they are legally authorized to work for Click Therapeutics in the U.S. and, if so, whether that authorization permits them to work in the job they seek.
In no case should Click Therapeutics support of a colleague's temporary visa application or sponsorship of a colleague for permanent residence be construed to guarantee success of that application or amend or otherwise invalidate the "at-will" employment relationship between the colleague and Click Therapeutics.