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Clinical Research Associate, Remote

£45,000 - £55,000

Hours: 40hpw (Mon - Fri)

Type: Permanent


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

  • Position will be filled at CRA or Sr. CRA level depending on experience and may include customer-managed clients.

  • 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.

  • Ability to perform regionalized travel an average of 65%, depending on project needs.

  • 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.

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