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)

Job Tags

Similar Jobs