Posted 8 months ago
Clinical Research Associate
Cambridge, Massachusetts, United StatesOn-siteContract
AI Summary
A Clinical Research Associate conducts site initiation, monitoring, and close-out visits, verifies study data, and collaborates with site staff to keep trials on track while addressing protocol, safety, and data issues.
About this role
Are you passionate about clinical research and ready to make an impact on patients’ lives? We’re looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company (confidential) that’s advancing innovative therapies in neuroscience.
What You’ll Do:
- Conduct site initiation, monitoring, and close-out visits to ensure trials meet the highest quality standards.
- Review and verify study data for accuracy and completeness.
- Collaborate with site staff and cross-functional teams to solve challenges and keep trials on track.
- Identify and escalate any protocol deviations, safety concerns, or data issues.
Requirements
What We’re Looking For:
- Bachelor’s in Life Sciences, Nursing, Pharmacy, or related field (advanced degree a plus).
- 3+ years of CRA or site monitoring experience.
- Strong knowledge of ICH-GCP and FDA regulations.
- Excellent communication, organization, and problem-solving skills.
- Willingness to travel as needed (up to 50–75%).
Extra Credit:
- Experience with CNS or rare-disease trials.
Benefits
Amazing benefits package starting day one!
Skills
CNS Or Rare-disease Trial ExperienceCrystal-clear DocumentationData VerificationFDA RegulationsICH-GCPProtocol AdherenceSite MonitoringTravel CoordinationTrial Management
