Who We Are

Click Therapeutics, Inc. develops and commercializes software as prescription medical treatments for people 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 is entering into a multi-center, randomized, controlled, parallel-group, phase III FDA registration trial for the treatment of Major Depressive Disorder in adults. Major pipeline expansion and progression is in process.

About the Role

The Clinical Research Coordinator (CRC) reports directly to the Associate Director, Clinical Operations.  This role is tasked with facilitating and coordinating early clinical research operations and the conduct of research and development clinical trials.  The Click Therapeutics in-house science and product teams routinely develop novel cognitive and neurobehavioral mechanisms of action for Click Therapeutics’ products as well as refine existing therapeutic approaches through targeted clinical research. 

The Clinical Research Coordinator works closely with the Scientists, Product Managers, Clinical Trial Managers, Clinical Research Associates and Click Technology teams to coordinate and execute research and development projects and clinical trials.  

This is a highly visible, creative, and agile role within a rapidly growing pre-IPO company in a nascent and fast-growing space. The role will be located in our trendy Tribeca HQ, includes great benefits, and is an excellent wealth-building/equity opportunity for the right individual.

Responsibilities

• Coordination of translational and discovery clinical research studies and clinical operations, including managing logistics, scheduling, timelines, deliverables, reporting requirements, documentation, and work plans for each project
• Assisting the Click Scientists and Study Leads with key project tasks, such as defining project scope, developing scopes of work and budgets, documenting study objectives, and overall helping to manage projects so they stay within scope, budget, and are completed on time
• Supporting study contact including preparing and submitting IRB and other research documentation as well as scheduling, coordinating and/or conducting study visits
• Coordinating work and outputs and facilitating communication internally
• Proactively identify and resolve and/or escalate study related issues
• Participate in project team meetings and conference calls to review progress of ongoing clinical trials
• Ensure the Clinical Trial File are maintained in an inspection-ready state
• Working closely with a great, close-knit team

Qualifications

• Bachelor’s degree required; degree in Psychology, Neuroscience or another scientific discipline preferred
• Clinical Research Coordinator 1-2 years’ experience, biotech, pharma, CRO setting, with medical, psychology, neuroscience clinical research preferred
• Working knowledge of Good Clinical Practice (GCP) and US and international regulations for clinical trials
• Advanced written, oral, and interpersonal communication skills, including proficient knowledge of medical terminology
• Ability to deliver results and execute on required activities individually, in a team setting
• Proven ability to work collaboratively and effectively in a team-based setting
• Excellent organizational skills and extraordinary attention to detail
• Tech savvy with confidence in the transformative potential of software as treatments
• Initiative, enthusiasm and a problem-solving approach to new challenges
• Systematic and efficient coordination skills, including an ability to prioritize

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.