Senior Clinical Trial Associate
Location: This position may be performed remotely, but requires the flexibility and willingness to travel as needed.
The Opportunity
At Praxis, our Senior Clinical Trial Associates are more than project coordinators—they’re builders, critical thinkers, and collaborators who help translate cutting-edge science into real impact for patients with CNS disorders. In this role, you’ll support the clinical team in driving trials forward—on time, with rigor, and always with the patient in mind. You’ll bring operational excellence, strong communication, and a bias toward action to every phase of the study lifecycle. This is a high-trust, high-impact role for someone who thrives in a fast-moving environment and is energized by doing things differently—and better.
Primary Responsibilities
- Support the Clinical team in the successful execution of clinical trials from protocol concept to clinical study report, complying with Good Clinical Practice (GCP) guidelines and international regulations
- Coordinate, provide set up, and attend project meetings including: internal team and CRO/ vendor meetings
- Set-up, update and maintain clinical trial-related trackers such as critical regulatory documents, trial master file (TMF), startup progress, screening/enrollment, study invoices/payments, project budgets, etc.
- Provide detail reviews for clinical trial documents, e.g. protocol, informed consent form, case report form
- Recognize and flag potential errors and deviations from timelines to CTM and team members
- Assist with IRB/EC and regulatory submissions
- Perform TMF reviews to ensure completeness and inspection readiness
- Regularly review documents to ensure adherence to Clinical Operations and/or project specific quality requirements (e.g. SOPs, work practices, training guides)
- Assist with identifying and implementing best practices and continuous improvement projects
Qualifications and Key Success Factors
- Bachelor’s degree in life sciences or healthcare field preferred. In lieu of degree, 4 or more years of relevant experience may suffice
- 2+ years of relevant hands-on drug development experience in Sponsor setting
- Knowledge of clinical trial operations, ICH, GCP Guidelines and other applicable regulatory requirements
- Excellent communication and organizational skills with experience working in a team across multiple functional areas, (e.g. Quality Assurance, Data Management, Biostats, Medical Writing, Safety, Clinical Supply, Finance)
- Intellectual curiosity, innovation and creative problem solving with an entrepreneurial spirit
- Ability to think critically in fast-paced projects with a keen sense of urgency and demonstrated ability to problem solve
- Self-motivated and able to work autonomously, as well as a member of a collaborative team
- Highly-organized and detail-oriented with a passion to deliver quality results
- Strong verbal and written communication skills with an ability to build relationships internally and externally
- The physical and mental requirements of our roles include but are not limited to regular use of a computer, devices or other office equipment, clear communication, and occasional movement. You'll need comfort with screen work, basic hand coordination, and focus. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.
Compensation & Benefits
At Praxis, we believe that taking care of our people (and their people) is important, so we provide a world class benefits package to help you thrive. This includes 99% of the premium paid for medical, dental and vision plans. We also provide company-paid life insurance, AD&D, disability benefits, and voluntary plans to personalize your coverage. Thinking about the future? We match dollar-for-dollar up to 6% on eligible 401(k) contributions and sweeten the deal with long-term stock incentives and ESPP. We provide a discretionary quarterly bonus, an extremely flexible wellness benefit, generous PTO, paid holidays and company-wide shutdowns. Not to mention, you'll also be joining a phenomenal crew of colleagues who are smart, engaged and inspiring. We aim high, collaborate hard, and produce results. Let’s achieve the impossible together!
To round out our world-class total rewards package, we provide annualized base salary compensation in the range listed below. Final salary range may be modified commensurate with job level, education, and experience.
Annualized Base Salary
$110,000 - $126,000 USD
Company Overview
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust, Ownership, Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members.
Diversity, Equity & Inclusion
Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE® to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws.
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