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Job summary
A clinical research organization is looking for a Clinical Trials Management Associate - III to handle site evaluations and ensure compliance with protocols. The ideal candidate should have over 4 years of relevant experience and a BS or BA in a scientific discipline or an RN certificate. The position is contract-based and offers flexibility for remote work, particularly for candidates located on the West Coast. The candidate should be adept in tools like Word, PowerPoint, and Excel.
Qualifications
4+ years of experience in clinical trials.
Experience in site evaluations and monitoring visits.
Must have knowledge of FDA and/or EMEA Regulations.
Responsibilities
Conduct site evaluations and routine monitoring visits.
Ensure compliance with protocols and regulatory requirements.
Assist in the preparation of safety and interim study reports.
Coordinate with CROs or vendors as needed.
Skills
Site evaluations
Regulatory compliance
Project coordination
Data analysis
Training
FDA regulations knowledge
Scheduling
Education
BS or BA in relevant scientific discipline
RN (2- or 3-year certificate)
Tools
Word
PowerPoint
Excel
Job description
A clinical research organization is looking for a Clinical Trials Management Associate - III to handle site evaluations and ensure compliance with protocols. The ideal candidate should have over 4 years of relevant experience and a BS or BA in a scientific discipline or an RN certificate. The position is contract-based and offers flexibility for remote work, particularly for candidates located on the West Coast. The candidate should be adept in tools like Word, PowerPoint, and Excel.