Clinical Research Associate (m/w/d)

Randstad Deutschland GmbH & Co. KG; Frankfurt; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A staffing agency is seeking a freelance Clinical Research Associate (CRA) near Frankfurt am Main. This role involves ensuring compliance with trial protocols and GCP regulations while conducting on-site and remote monitoring of clinical trials. The ideal candidate will have a degree in Life Sciences, proven experience in the Pharma/Biotech sector, and the ability to maintain high analytical and communication standards. Flexible payment and contract options are offered.

Leistungen

Attractive payment options

Fast, reliable payment of fees

Electronic signature for contracts

Qualifikationen

• Proven professional experience as a Clinical Research Associate (CRA) in Pharma/Biotech.
• Comprehensive knowledge of GCP, ICH Guidelines, and national laws.
• Strong analytical and detail-oriented work approach.

Aufgaben

• Ensuring compliance with trial protocol, GCP, and regulatory requirements.
• Performing Source Data Verification (SDV) (CRF vs. source patient data).
• Generating precise site visit and communication reports.
• Diligent documentation in the Trial Master File (TMF).
• Identifying and resolving deviations, discrepancies, and errors (Query Management).
• Conducting On-site/Remote Initiation, Monitoring, and Close-out Visits.

Kenntnisse

Monitoring clinical research projects

Source Data Verification (SDV)

Regulatory compliance

Analytical skills

Communication skills

Ausbildung

Degree in Life Sciences, Medicine, Pharmacy

Jobbeschreibung

We are looking for anexperienced freelance Clinical Research Associate (CRA)to strengthen our client's project Team near Frankfurt am Main. Your expertise inmonitoring clinical research projectsacrossPhases I-IVis crucial for overseeing and ensuring the quality of clinical trials.Your expertise is in demand! Apply now.

Ihre Aufgaben

• Ensuring compliance with trial protocol, GCP, and regulatory requirements
• Performing Source Data Verification (SDV) (CRF vs. source patient data)
• Generating precise site visit and communication reports
• Diligent documentation in the Trial Master File (TMF)
• Close collaboration, training, and clarification with Investigators/site personnel
• Identifying and resolving deviations, discrepancies, and errors (Query Management)
• Conducting On-site/Remote Initiation, Monitoring, and Close-out Visits

Erfahrungen

• Degree in Life Sciences, Medicine, Pharmacy, or comparable
• Proven professional experience as a Clinical Research Associate (CRA) (Pharma/Biotech)
• Comprehensive knowledge of GCP, ICH Guidelines, and national laws
• Strong analytical and detail-oriented work approach
• Excellent communication and organizational skills

Das bieten wir Ihnen

• Attractive options for shortening your personal payment term
• No more time-consuming invoicing
• Fast, reliable payment of fees
• Conclude project contracts by means of electronic signature