Description
The clinical research associate monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs, and study protocols.Primary Duties
- Review regulatory documents as required and prepare site visit reports. Responsible for multiple projects and must work both independently and in a team environment.
- May participate in the study development and start-up process including reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project-specific CRA training.
- May participate in clinical training programs and maintain awareness of developments in the field of clinical research as needed.
Requirements:
- Phase 1 experience
- Prefer BS/BA- 2 yrs monitoring experience or combination of on-site monitoring and clinical research coordinator experience
- Customer service orientation
- Sound knowledge of medical terminology and clinical monitoring process
- In depth therapeutic and protocol knowledge as provided in company training
- Excellent verbal and written communications skills
- In depth therapeutic and protocol knowledge as provided in company training
- Excellent interpersonal and organizational skills and attention to detail Computer literacy, proficiency in MS Office.
This is an excellent opportunity to work for a fast moving organisation, offering competitive daily rates. If you are interested in this position and would like some more information please send an updated CV and call Hailey on .
Please also pass this opportunity onto anybody you know who may be interested in this as we do offer £250 referral vouchers.
Have a lovely day and I look forward to hearing from you.