CRA URGENTLY REQUIRED - FRANCE

Job Type:
Permanent
Sector:
Clinical Research
Job Category:
CRAs
Region:
Europe
Area:
France
Location:
Unspecified
Salary Description:
Competitive Salary Offered
Posted:
11/11/2016
Job Ref:
LZBUCRAFRA

My client is seeking to appoint a Clinical Research Assistant (CRA) in France with at least two years’ independent monitoring experience.

 Requirements and Qualifications:

·         Relevant life science medical / nursing degree or relevant degree or background preferred.

·         Customer service orientation.

·         Sound knowledge of medical terminology and clinical monitoring process.

·         Excellent communication in English in both written and verbal skills.

·         Computer literate and proficient in Microsoft Office.

·         Excellent interpersonal and organizational skills.

·         Ability to work independently and to effectively prioritize tasks.

 Key Responsibilities:

  • Monitor clinical trials to ensure absolute adherence to Good Clinical Practice in accordance with ICH-GCP standards.
  • Site management to ensure proper adherence to protocol, source data verification and assess CRF entries
  • Develop, review and edit clinical trial related documentation including but not limited to; Case Report Forms, Informed Consent Forms, study specific handbooks, guidelines and checklists
  • Assist with study protocol design, development and / or review if required
  • Perform pre-study initiation, interim monitoring and close out visits as required
  • Carry out drug formulation administration procedures and documentation records
  • Ensure adequacy of drug shipment and drug accountability

If you are interested in this role please contact directly at lbrunaud@barringtonjames.com / +44 (0)1293 776644.

Contact Details:
Tel: 01293 776644
Contact: Liz Brunaud
Email:

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