|20.10.2022||France||Degree in Life Sciences|
|Expiry Date||Gender||Job Category|
An international pharmaceutical company with a strong focus on research and more than 85 years of experience is looking for a Clinical Trial Transparency & Documentation Specialist to help with the implementation and upkeep of the Clinical Trial Disclosure requirements and to serve as the GCD Department’s key user and subject matter expert for EDMS, supporting the management activities for clinical studies documentation throughout the documents life-cycle.
With more than 6,000 workers and operations across 30 countries, our client’s R&D division is a key resource for the company.
You would join a company that firmly believes that its employees are its most valuable asset and, as a result, invests in ongoing training, learning, and development, creating a dynamic, quickly-growing, challenging, and friendly workplace.
Since the position is an internal replacement, you will have excellent prospects for professional advancement.
serves as a subject matter expert on the prerequisites for clinical trial registration and posting of summary results; coordinates the registration of clinical trials on the website ClinicalTrials.gov; carries out cross-functional and cooperative planning, coordination, and management of the global transparency activities (posting of summary results in EU/US registries, Lay Summaries results for Patients and the General Public, Clinical Data Sharing, and other transparency-related activities in the EU, US, and third countries);
A position in clinical study management or at least two or three years doing comparable duties in an R&D context * Transparency and documentation
- Master’s degree or equivalent academic credential in the life sciences
- Perfect English (French not required)
- Knowledge of clinical trials, a regulatory mindset, and IT expertise
If you’re interested, please contact Anna Di Martino at
with a word version of your resume.
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made on October 20, 2022, by NonStop Consulting