Clinical Contractors

Job type:
Start date:
6 months
Real Staffing
City of London
Published at:
flag_no United Kingdom
Project ID:

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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.

  • 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.