SENIOR CLINICAL TRIAL ASSISTANT, PROJECT ADMINISTRATOR, PARIS, CLIENT DEDICATED

Job Overview:

Covance are still actively hiring throughout the COVID-19 outbreak

We continue to support and meet the needs of our clients by initiating new studies from Early Development through Phase IV, our Central Labs are fully operational and we have just received FDA approval to perform COVID19 tests using an at-home collection kit.

Across the globe, we keep intact our commitment to improve health and improve lives, and are looking for exceptional people who are eager to play an important role pushing new frontiers in how we diagnose, monitor and treat patients.

In France, our sponsor dedicated team continues its expansion, and we have several job opportunities for experienced Clinical Trial Assistants / CTA / Clinical Project Administrators / CPA.

The Clinical Trial Assistant CTA CPA job

  You will work sponsor dedicated for a prestigious Top 5 global Pharmaceutical company (mainly in Oncology , but also Vaccines, Infectious diseases, Cardiology and Neurology).

  These jobs are office based in the Paris Area .

Among your main responsibilities, you will:

 Provide support to the Projects Managers (Billing follow up, proofreading and editing correspondence, large and small documents, mailings, shipment of study files, fax and photocopy documents, assemble study documents, and arrange meetings, etc.) Provide support with Contracts Set up and maintain clinical investigator files and documentation Data entry and maintenance of selected study tracking databases Prepare monitoring visit documentation for Clinical Research Associates Prepare study-related documents and other materials for delivery to archives, at appropriate intervals Perform other administrative duties as assigned by management

WHAT MAKES THESE JOBS SPECIAL

  You will join a successful and stable project team: last year we almost doubled our team in France.

OTHER INFORMATION

This role is a full time & permanent position to be employed through Covance. For more information please contact Carlos Villanueva on +34 648 853 615   or mail carlos.villanueva@covance.com

COVANCE ARE PRACTICING SOCIAL DISTANCING WITH VIDEO INTERVIEWS

All your interviews with us will be conducted via phone or using WebEx video. To help you prepare, check out this brief guide for best practices and WebEx guidance:

https://www.labcorp.com/labcorp-enterprise-video-interviewing-guide Education/Qualifications:

B.A./B.S. (Life Science preferred) or equivalent healthcare experience

French and English Experience:

This is not an entry level role, and since you will be assigned to complex clinical trials we need you to bring min 2 years experience in a similar position at biopharmaceutical or CRO companies, so you have developed skills in the following areas:

  Ability to support preparation of submission package for IRB/ERC and support regulatory agencies submissions Site administration (i.e., tracking essential documents and safety reporting) Collating, distributing, and archiving study tools and documents Use of clinical trial databases (CTMS) and study trackers Preparation of study documents, and correspondence with sites eTMF reconciliation Investigator trial file binders preparation eTMF Quality Control Plan