Senior Clinical Research Associate

Recruiter
Clinical Professionals
Location
South East England
Posted
02 Dec 2017
Closes
07 Jan 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Senior Clinical Research Associate
South East
Field based or Office Based in Middlesex
Competitive salary and benefits + car allowance

My client, a global CRO, are looking for an experienced CRA/SCRA to join their fast growing team on a permanent basis. You will be monitoring sites nationwide and approximately 2 days per week.

Responsibilities;
*Monitoring full lifecycle of clinical trials.
*Site initiation visits.
*Ensure all trial documentation is in line with study protocol, GCP and regulatory requirements.
*Ensure documentation is correctly filed in the TMF (Trail Master File).
*Review and report protocol/GCP/SOP deviations.
*Site closure visits.

Candidate Requirements;
*12 months independent monitoring/co-monitoring experience
*Ability to travel Nationwide
*Full UK driving license
*Life science degree

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