Senior Clinical Research Associate

Proclinical are recruiting for a Senior Clinical Research Associate for a CRO. This role is on a permanent basis and is located in France.

Responsibilities:

• Perform qualification, initiation, supervision and close-out visits for research sites in compliance with the approved protocol.
• Guarantee GDP are being adhered to and discussing protocol deviations suitably per SOPs, GCP and suitable regulatory needs.
• You will verify and evaluate adverse events, serious adverse events, concomitant medications and equivalent illnesses to confirm precise data reporting rendering to the protocol.
• Examine the clinical research site's patient recruitment and retention success and offering proposals for improvement.
• Accomplish supervision reports and follow-up letters, which involves offering summaries of the significant discoveries, deviations, deficiencies and suggest actions to secure compliance.
• Other duties may be assigned.

Key Skills and Requirements:

• Familiarity in a clinical research associate role.
• Willing to travel for business needs up to 60-80% of the time.
• Educated to a degree level in a health or scientific discipline.
• Computer literacy in MS Office.
• Fluency in both he French and English languages.
• Communication skills both verbally and in writing.
• A high attention to detail with the ability to manage own time efficiently.

If you are having difficulty in applying or if you have any questions, please contact Auxanne Rameix at +44 203 954 7011.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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