Clinical Trial Associate

An established biopharmaceutical company is currently recruiting a Clinical Trial Associate to join their team in France. The company is focussed on the discovery and development of innovative therapeutic and diagnostic solutions in chronic diseases where there are considerable unmet medical needs. This is an exciting opportunity to bring expertise and skills to an established and in-demand company.

Job Responsibilities:

• Assisting all the Clinical Development teams in the preparation, processing, classification, archiving and monitoring of clinical documentation (paper and electronic) and various reports.
• Ensuring the organisation and management of electronic clinical study files (eTMF) from an organisational point of view (rigorous classification) and from a qualitative point of view (verification of the quality of the elements preserved and preparation of reports regular advancement).
• Guarantee the update and monitoring of internal trackers for ongoing clinical trials and study documentation.
• Be the administrative referent of the Clinical Development department for external service providers (notably Contract Research Organisations, CROs), and internal departments involved in clinical trials.
• Using the tools made available and / or develop tracking tools to provide key indicators and provide administrative support when necessary.
• Participating in the development of internal processes and procedures for the proper management of the TMF (Clinical Trial Master File).
• Represent the Clinical Operations team for certain communications or associated documentation for current projects.
• Organising and participating in internal team meetings, preparing the agenda and writing the minutes.

Skills and Requirements:

• Minimum Bac +3 diploma and you have at least 2 years of experience in Clinical Operations.
• Use the Office Pack daily (Word, Excel, Powerpoint) as well as clinical trial management tools (Veeva Vault eTMF preferably).
• Excellent knowledge of Good Clinical Practices (GCP, GCP).
• Perfect command of English, both written and spoken, in a professional context. An identical level of mastery for French is a plus. At a minimum, you express yourself correctly and easily in English, both in writing and orally in your area of competence.
• Demonstrate a very strong ability to adapt, organise and manage priorities.
• Your thoroughness, your discretion and your sense of confidentiality are recognised and appreciated.
• Create and maintain effective working relationships with your colleagues, managers and external contacts.
• Demonstrable multitasking, project management, and execution skills.
• Good interpersonal skills, including communication, presentation, persuasion, and influence.
• Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
• Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Patrick Aguie at 0203 854 1077 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

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

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