Senior Global Clinical Project Manager

Senior Global Clinical Project Manager

My client is an innovating, dynamic and niche international biopharma company currently expanding their clinical development team based in Vaud Canton.

Due to this growth my client is looking for a Senior International Clinical Project Manager with strong experience at a global level (including US Europe or Asia)

Your responsibilities :

  • Lead the overall initiation, coordination, implementation and management of large international clinical trials from start-up to close out.
  • Lead the cross functional study team dedicated to the clinical study to ensure clinical program goals and timelines are met;
  • Manage operational and technical aspects of projects including budgeting, study initiation and risk management;
  • Anticipate potential issues and risks within the clinical program, create contingency plans and drive solution implementation;
  • Assist in the identification of investigational sites and coordinate co-monitoring with CRAs when required;
  • Represent clinical operations on multi-function project teams internally and externally; report on study progress;
  • Establish study milestones and ensure accurate tracking and reporting of study metrics and timelines, alert in case of deviations or risks, and propose mitigation plans;
  • Provide operational input (and scientific if appropriate) into Protocol synopsis, Study protocol and all other study related documents;
  • Select, manage and coordinate external vendors, such as Contract Research Organizations (CROs), central laboratories, etc;
  • Monitor vendor and CROs performance and ensure continuous oversight;
  • Design, review and approve of all trial related documentation, and establish trial processes.

Your profile :

  • University degree or equivalent in Life Sciences.
  • Fluent in English – French is an asset  
  • 8-10 Years experience in Clinical Project Management roles
  • Proven track record of successful management of large complex clinical trials in the Pharmaceutical Industry or CRO.
  • Deep knowledge and experience on the implementation and use of EDC, IWRS, eTMF, CTMS and any other digital clinical trial systems.
  • Experience in management of CROs, vendors and consultants.
  • Strong project management skills.
  • Excellent budgeting, planning, and communication skills.
  • Ability to lead and influence a cross-functional study team and external partners.
  • Willingness to travel up to 10-30%

To apply please send your CV to noliva@axepta.com

Noemie Oliva noliva@axepta.com

Noemie a plus de 7 ans d'expérience en recrutement de professionels dans le domaine pharmaceutique et médical en Suisse, France et en Belgique. Spécialités: recherche proactive, publicité ciblée, professionnalisme, réseautage, recrutement permanent, recrutement de freelance, emplois difficiles à remplir, postes vacants multiples, postes vacants urgents Si vous souhaitez avoir une discussion confidentielle concernant votre recherche de personnel ou votre recherche d'un nouveau poste, n'hésitez pas à me contacter directement à noliva@axepta.com