Clinical Project Manager Setup M/F - FR

KAYENTIS is a software solutions provider specialized in clinical trials.

Our core competence is in patient data capture and processing solutions (eClinical Outcome Assessments = eCOA) and we are now expanding towards Decentralized Trials functionalities.

With 16 years of global experience in eCOA, Kayentis has supported more than 260 clinical trials in 79 countries with more than 90,000 patients. Its head office is located in Meylan, near Grenoble (France), Kayentis is also present in Boston (USA) and Tokyo (Japan).

Joining Kayentis' teams means choosing a fast-growing company committed to improving clinical trials and the well-being of its employees.

KAYENTIS is growing! Develop your career with us! Join an international, cohesive and dynamic team and develop new skills!

KAYENTIS is growing! Develop your career with us!

Join an international, cohesive and dynamic team and develop new skills!

For more information about Kayentis, visit our career page, or have a look at our employee satisfaction survey results. Make sure to follow us on the social media platforms for our latest news and updates: Twitter, Facebook, LinkedIn and Instagram.

The Clinical Project Manager ‘Set Up’ permanent position is based in Meylan (nearby Grenoble 38)

The Context:

Reporting to the Business Unit Manager, you are responsible for the delivery and set-up of adapted solutions require by our clients, respecting regulations and quality procedures.

• You are responsible for the successful implementation of the project from specifications to delivery.
• You are the primary point of contact for the client from contract award throughout the setup.
• You are participating to pre-sales meetings supporting the sales team.

YOUR MISSION :

• Manage the communication with the sponsor, CRO and other actors involved in the project.
• Specify and assess client needs and, in conjunction with the technical teams, consolidate the project plan and specification documents.
• Coordinate the communication internally with a cross-functional project team and external partners.
• Lead the planning, project tasks, and ensure deadlines are met.
• Prepare the validation process and lead the sponsor Usability Acceptance Testing (UAT).
• Identify the risks on the project, follow issues and manage alongside the sponsor the definition of related action plans.
• Report to Sales any change related to the scope of the project. Evaluate the related cost impacts.
• Conduct customer and end user training.
• Participate in drafting and updating the project and quality documentation.

YOUR PROFILE:

Degree in related field (B.S, M.S. or Pharm.D.), you have minimum 5 years of experience in clinical research and/or similar role within pharmaceutical sector in biotechnologies.

• Proven experience in the domain of clinical trials
• Project management skills
• Excellent communication skills and writing skills, good team player
• Rigorous, organized, customer-focused, self-starter

YOUR BENEFITS:

• Flexible working hours
• Bonuses
• Meal tickets
• Bike allowance

Are you interested in this opportunity? >> Contact us and send us your CV at career@kayentis.com <<