Who We Are:

Click Therapeutics, Inc. develops, validates and commercializes software as prescription medical treatments for patients with unmet medical needs. Through cognitive and neurobehavioral mechanisms, Click’s Digital Therapeutics™ enable change within individuals, and are designed to be used independently or in conjunction with biomedical treatments. The Clickometrics® adaptive data science platform continuously personalizes user experience to optimize engagement and outcomes. Following a groundbreaking clinical trial, Click’s industry-leading smoking cessation program is available nationwide through a wide variety of payers, providers, and employers. Click’s lead prescription program has entered a pivotal, fully remote, randomized, controlled trial on the Verily platform for the treatment of Major Depressive Disorder (MDD) in up to 540 adults. Click is progressing a broad pipeline of Digital Therapeutics™ across a variety of high-burden therapeutic areas, including MDD, Schizophrenia, Migraine, Chronic Pain, Atopic Dermatitis, Acute Coronary Syndrome (ACS), Obesity and more.

Responsibilities:

• Provide medical affairs, medical scientific affairs leadership with oversight of the medical scientific affairs aspects of Click’s areas of focus in Neurology and Psychiatry.
• Provide scientific and medical/clinical advice when necessary to relevant stakeholders both inside and outside of the organization.
• Present healthcare professionals and decision makers with accurate, unbiased, balanced and timely answers to unsolicited request for information about Click’s products.
• Design, develop, manage, analyze, interpret, write, present, and publish Phase 4 clinical, outcome, registry and non-clinical studies.
• Provide study support from protocol review and budget review to submission and completion for Investigator Initiated Trials (IIT’s).
• Support payer reimbursement by providing clinical information and insight.
• Develop and deliver very specialized scientific/educational programs including but not limited to formulary presentations for managed care and related organizations.
• Provide continuing field scientific support and training for sales, MSL’s and Corporate Account Managers (CAM’s).
• Develop and execute scientific association, thought-leader, and publication strategies based on the Medical Affairs Strategic Plan.
• Contribute to drug safety assessments when necessary, reporting and quality assurance.
• Develop medical scientific affairs strategy in conjunction with functional leadership and develop topics and compile data for descriptive and teaching presentations.
• Assist Medical Affairs / Medical Scientific Affairs as well as agency personnel in the development of presentations and slide kits for Click’s products.
• Contribute scientific, clinical, and experiential insights to the IIT, CME, and grant review processes.
• Participate in multidisciplinary and global projects to support commercialization, including promotional and labeling review to examine material for scientific accuracy.
• Create, develop, and enhance relationships with the medical community; plan, organize, conduct, and lead expert panels, consultant and advisory meetings, in cooperation with marketing.
• Actively participate in advisory boards, speaker training events, clinical investigator meetings, regional national and international meetings when required.
• Support Medical Information in addressing product questions from consumers and health care professionals; assist Ferring colleagues with physician communications.

Qualifications:

• D., PharmD or PhD with other Advanced Degrees considered.
• 3+ years of Pharma experience within therapeutic area or relevant research experience.
• Experience in Medical Affairs product planning and development involving publication strategies, product monographs, promotional materials and/or drug safety surveillance preferred.
• History of publication of peer-reviewed publications demonstrating ability to organize, analyze, and interpret clinical/non-clinical data a plus.
• Experience in Pain, Neurology, Psychiatry or associate fields preferred.
• Tech savvy with confidence in the transformative potential of software as treatments.
• Experience executing translational cognitive and behavioral research.
• Record of scientific publication and presentation.
• Ability to develop medical/scientific data into clear, cogent vignettes, teaching programs, and plenary presentations.
• Commitment to provide leadership by example.  

Benefits:

Stock options | Competitive salary with annual review | 401(k) matching | Annual performance-based cash bonus | Comprehensive medical benefits through Aetna | Flexible Spending Accounts | Life insurance and disability benefits | Open vacation policy / unlimited PTO | Generous paid parental leave | Commuter subsidies | Monthly catered lunches | Choice of Mac, Windows, or Linux equipment | Sponsored company events | Free, unlimited office snacks and beverages | Much more…

Equal Employment 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.