Clinical Research Associate/Regional CRAs
Description:
The clinical research associate position may be at our office or home-office-based. Primary responsibilities include:
- Conducting site visits to determine protocol and regulatory compliance
- Preparing required site visit and documentation reports
- Developing collaborative relationships with investigative sites and customer company personnel
Requirements:
- Bachelor's degree in life science, nursing, a related field or equivalent experience
- A minimum of two years of monitoring experience or two years clinical experience in medical research, nursing or the pharmaceutical industry
- Knowledge of GCPs and FDA regulatory requirement and guidelines for clinical monitoring
- Effective clinical monitoring skills, management skills or core therapeutic expertise
- Experience conducting qualification, initiation, interim and close-out visits
- Position involves extensive travel (about 50% of work time)
To apply for the above positions, please submit your résumé or curriculum vitae (CV) to careers@researchpoint.com.