Clinical Project Manager
Date: 17 sept. 2024
Teoxane Laboratories were established in Geneva, Switzerland, in 2003. They are specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and dermocosmetics. Teoxane's strength is to offer global patient care. Using its products, practitioners can fill all kinds of wrinkles, from the finest to the deepest, to restore youthful volume to the face, and to treat the neck and décolleté, with natural results. The strength of Teoxane is also its human size and independence, allowing for freedom of thought, action, and innovation which makes the company unique.
Main activities
* Implement, execute and complete clinical research projects sponsored by Teoxane according to timelines and budget.
* Be responsible for compliance with local regulations, GCP regulations, and internal SOPs in clinical projects.
* Work cross-functionally within Teoxane departments to prepare required study documentation for submission to Ethics Committees and competent authorities, including oversight, writing, and review of documents.
* Develop and manage the overall clinical study budget.
* Select and validate investigator/site, and vendors (i.e., CROs).
* Contribute to the negotiation and preparation of contracts and budgets with third parties and sites participating in our studies.
* Responsible for the development of high-quality study documentation (i.e., from study protocol and study plans to final clinical study report) throughout the clinical study.
* Manage Contract Research Organizations (CROs) and third-party vendors, ensuring adherence to scope of work within timelines and budget.
* Work cross-functionally within the clinical team to monitor site performance (such as enrollment and compliance with study protocol), ensuring high-quality data collection and review in clinical projects.
* Ensure that all relevant documents are properly and timely archived in the TMF during the study.
* Participate in internal process improvements.
Your profile
* Minimum B.Sc. degree in a relevant scientific discipline (e.g., Biochemistry, Microbiology, Pharmacy, Biological Sciences, or Related Pharmaceutical Science).
* Minimum of 4 years of experience in clinical operations; project management skills.
* Experience in the industry, especially in medical device clinical trials, is a plus.
* Strong critical thinking and problem-solving skills.
* Strong negotiation, communication, and presentation skills across all levels.
* Able to rapidly adapt to changing environments and circumstances.
* Fluent in English and French.
If you decide to apply for this position, you must read the Candidate Privacy Policy (Access to the link). You may exercise the various rights regarding your data described therein at any time, in accordance with the procedures set forth in it.
TEOXANE promotes equal opportunity and places at the heart of its human resources management policy the fight against all forms of discrimination based on age, gender, origin, disability, or any other personal characteristic.
#J-18808-Ljbffr