Senior Clinical Research Associate
New
W
Worldwide Clinical TrialsClinical Research
England, United KingdomFull-TimeSenior
Salary not disclosed
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Job Details
- Languages
- English
- Experience
- 5+ years of experience as a Clinical Research Associate
- Required Skills
- Microsoft Office
Requirements
- 5+ years of experience as a Clinical Research Associate.
- 4-year university degree or RN/BSN in Nursing.
- Proficiency in Microsoft Office, CTMS, and EDC Systems.
- Excellent interpersonal, oral, and written communication skills in English.
- Superior organizational skills with attention to details.
- Ability to work with little or no supervision.
- Willingness to travel.
Responsibilities
- Execute site qualification, initiation, interim monitoring, site management, and study close-out visits.
- Provide mentoring and guidance to less experienced CRAs and site staff.
- Document site visit findings via written reports.
- Assess, monitor, and train study site staff on protocol adherence.
- Review study subject safety information and informed consent.
- Conduct source document verification for compliance and patient safety.
- Review CRFs using paper or electronic data capture systems and assist with data query resolution.
- Update site-related documentation for the Trial Master File (TMF).
- Ensure site compliance with IP receipt, accountability, and return or destruction.
- Conduct accompanied site visits for assessment or training of other CRAs.
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