Job Description
Job Title: Clinical Research Associate
Location: Alameda, CA 94502 (100% Onsite)
Duration: 6 Months (High chance of extension)
Key Responsibilities:
- Monitor and oversee clinical trial sites.
- Ensure study compliance with protocols and regulations.
- Support and train investigators and study coordinators.
- Identify and resolve study-related issues and data discrepancies.
- Maintain clinical documentation (protocols, CRFs, reports, etc.).
- Support onboarding and training of new CRAs.
- Communicate site updates and escalate risks as needed.
- Manage CROs/vendors for outsourced activities.
- Ensure adherence to GCP, SOPs, and regulatory standards.
- Collaborate cross-functionally (e.g., QA, Compliance, Product Dev).
Qualifications:
- Education: Bachelor's degree in Biology, Health Sciences, Math, Computer Science, or related field.
- Experience: Previous experience in Clinical Research/Trials required.
- Skills:
- Strong understanding of clinical processes and monitoring
- Independent, proactive, and adaptable
- Critical thinker with strong communication skills
- Certifications: CCDM or similar (nice to have, not required)
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