In-House Clinical Research Associate (CRA)
Praxis Precision Medicines, Inc.
August 17, 2026
Remote
United States
Clinical Research and Development
This position may be performed remotely but requires flexibility and a willingness to travel as needed.
Position Summary
In-House Clinical Research Associate (CRA) to help execute fast, high-quality clinical trials, ensuring studies are inspection-ready and run with rigor.
Primary Responsibilities
- Support study execution by managing meeting logistics, documenting decisions, and tracking action items.
- Partner with Clinical Operations and site monitors to ensure protocol compliance and quality standards.
- File site-level documents into the Trial Master Files (TMFs) in a timely manner.
- Track, review, and organize essential documents from sites and vendors.
- Identify, escalate, and help resolve site-level issues with cross-functional teams.
- Assist with regulatory submissions and other study deliverables.
- Drive process improvements to enhance speed, quality, and patient impact.
Qualifications / Key Success Factors
- Bachelor’s degree in a life science/health-related field (or equivalent experience).
- 5+ years of clinical trial experience (biotech, pharma, or CRO).
- Solid knowledge of GCP, ICH guidelines, and regulatory requirements.
- Exceptional organizational and communication skills.
- Proactive, problem-solving mindset with high attention to detail.
- Comfortable managing multiple priorities in a fast-paced environment.
- Strong team player in flat, agile organizations.
- Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook).
- Ability to perform regular computer/device work and occasional movement (reasonable accommodations may be made).
Compensation & Benefits
- Annualized Base Salary: $75,000–$95,000 USD
- 99% of premium paid for medical, dental, and vision; company-paid life insurance, AD&D, disability; voluntary plans
- 401(k) match up to 6%; long-term stock incentives and ESPP; discretionary quarterly bonus; flexible wellness benefit; generous PTO, paid holidays, and company-wide shutdowns.
Position Summary
In-House Clinical Research Associate (CRA) to help execute fast, high-quality clinical trials, ensuring studies are inspection-ready and run with rigor.
Primary Responsibilities
- Support study execution by managing meeting logistics, documenting decisions, and tracking action items.
- Partner with Clinical Operations and site monitors to ensure protocol compliance and quality standards.
- File site-level documents into the Trial Master Files (TMFs) in a timely manner.
- Track, review, and organize essential documents from sites and vendors.
- Identify, escalate, and help resolve site-level issues with cross-functional teams.
- Assist with regulatory submissions and other study deliverables.
- Drive process improvements to enhance speed, quality, and patient impact.
Qualifications / Key Success Factors
- Bachelor’s degree in a life science/health-related field (or equivalent experience).
- 5+ years of clinical trial experience (biotech, pharma, or CRO).
- Solid knowledge of GCP, ICH guidelines, and regulatory requirements.
- Exceptional organizational and communication skills.
- Proactive, problem-solving mindset with high attention to detail.
- Comfortable managing multiple priorities in a fast-paced environment.
- Strong team player in flat, agile organizations.
- Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook).
- Ability to perform regular computer/device work and occasional movement (reasonable accommodations may be made).
Compensation & Benefits
- Annualized Base Salary: $75,000–$95,000 USD
- 99% of premium paid for medical, dental, and vision; company-paid life insurance, AD&D, disability; voluntary plans
- 401(k) match up to 6%; long-term stock incentives and ESPP; discretionary quarterly bonus; flexible wellness benefit; generous PTO, paid holidays, and company-wide shutdowns.