Clinical Trial Associate

📋 Description

• Support Phase 1-3 trials: activation, conduct, and closeout.
• Manage TMF setup, maintenance, and QC for inspection-readiness.
• Collaborate with CROs to review monitoring reports, deviations, and KPIs.
• Coordinate with internal teams and vendors to meet regulatory requirements.
• Assist in collection and review of regulatory documentation for initiation.
• Organize study meetings, logs, and documentation of progress.

🎯 Requirements

• Bachelor’s degree; life sciences or related degree preferred.
• 6 months to 1 year of Phase 1-3 clinical trial experience (sponsor or CRO).
• Proficient in eTMF and CTMS; knowledge of FDA and ICH-GCP.
• Strong organizational skills, problem solving, and communication.
• Understanding of clinical drug development; study design.
• MS Office proficiency (Word, Excel, PowerPoint).

🎁 Benefits

• Competitive benefits package.
• Eligible for annual bonus and equity.
• Opportunity to contribute to pivotal trials and regulatory submissions.