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Job summary
A leading IT staffing firm is seeking a Clinical Research Associate to implement and execute phase I-III clinical trials. The role involves ensuring compliance with regulations, collaborating with Clinical Study Teams, and developing new clinical investigator sites. Ideal candidates will have at least nine years of experience, proficiency in Microsoft Office, and experience with EDC and Clinical Trial Management Systems. This position requires travel of approximately 60% and strong communication skills.
Qualifications
Minimum of nine years related experience.
Five years of direct regional field clinical monitoring/research.
Currently working in regional position from established home office is preferred.
Responsibilities
Implement and execute client’s phase I-III clinical trials.
Ensure compliance with regulations, guidelines, and policies.
Support budget and contract negotiation with investigational sites.
Collaborate with Clinical Study Teams to resolve site issues.
Train and qualify sites and Principal Investigators.
Skills
Microsoft Office proficiency
Electronic Data Capture (EDC) System Experience
Clinical Trial Management System Experience
Excellent verbal and written communication
Problem-solving skills
Team orientation
Education
Degree in Medical, Pharmaceutical, Biology, Chemistry or RN
Tools
Medidata RAVE
Medidata CTMS
Job description
A leading IT staffing firm is seeking a Clinical Research Associate to implement and execute phase I-III clinical trials. The role involves ensuring compliance with regulations, collaborating with Clinical Study Teams, and developing new clinical investigator sites. Ideal candidates will have at least nine years of experience, proficiency in Microsoft Office, and experience with EDC and Clinical Trial Management Systems. This position requires travel of approximately 60% and strong communication skills.