clinical project manager à Plan-les-Ouates

publié
contact
Angèle Atlan, Genève Professionals Health Care & Life Sciences
type d'emploi
placement fixe
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job details

publié
lieu
plan-les-ouates, genève
secteur
life sciences
type d'emploi
placement fixe
référence
15586
contact
angèle atlan, genève professionals health care & life sciences
téléphone
058 201 54 40

description du poste

We are looking for our client, a growing and dynamic medical device company in Geneva, for a Clinical Project Manager.You will be responsible for leading, planning, implementing and delivering post market clinical trials on medical devices used in surgery.You are responsible to ensure that studies are carried out according to the protocol, SOPs, applicable regulations and principles of Good Clinical Practice. 

Your tasks:

  • You lead the assigned clinical trials from start-up to closure.

  • You establish study milestones and ensure accurate tracking and reporting of study metrics and timelines.

  • You coordinate the study protocol and report development.

  • You anticipate potential issues and risks within the clinical studies, create contingency plans and drive solution implementation.

  • You manage site selection process and site communication throughout the studies.

  • You design, review and approve trial related documentation. 

  • You collaborate with clinical data management and statistics in developing case report forms, managing data clean-up, and analysing study data.

  • You manage Contract Research Organizations (CROs), image laboratories, etc.

  • You coordinate co-monitoring with CRAs when required.

Your profile:

  • You have a university degree or equivalent in Life Sciences.

  • You have mininum 6-8 years of experience as a Clinical Trial Project Manager in the Medical Device Industry. 

  • You have excellent Project Management skills, including clear and proactive communication, budgeting, timelines, issues and risk management.

  • You are experienced in coordinating protocol development.

  • You are experienced in safety reviews and report writing is desirable.

  • You are experienced in management of CROs, vendors and consultants.

  • You are Fluent in English, French is a plus. 

  • Willingness to travel (approximately 25%).