Clinical Research Associate

Recruiter
S E C Recruitment Limited
Location
London (Greater)
Posted
10 Feb 2018
Closes
15 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
An European CRO which is expanding its operations in the UK is looking for 3 permanent CRAs to manager studies conducted across UK.

Responsibilities:
You will be responsible for the identification, qualification and initiation of investigators and their sites. You will supervise study conduct according to GCP requirements and all applicable laws.
You will be responsible for performing and coordinating all aspects of the clinical monitoring process from "start up" to "close out" on international studies.
Regulatory submissions ( EC, MHRA etc)
You will be involved in co-monitoring and mentoring of junior CRAs.

Requirements:
Education in Life Sciences Degree, Pharmacy or Medicine:

*1 - 5 years previous experience as CRA within a CRO, pharma, Biotech or device company
*Knowledge of ICH and GCP guidelines including a basic understanding of regulatory requirements.
*Ability to handle multiple tasks to meet deadlines is essential.
*Previous experience working as a CRA
*Proficiency in Microsoft Office Suite required.
*Excellent communication skills
*A full clean driver's license

for more information please contact me on Email address removed or Phone number removed

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