Clinical Project Manager M/F

Kayentis

Cambridge, MAFull-timePosted Apr 11, 2026

Behavioral Health Market Context

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Benefits

Health InsuranceDental Coverage

Job Description

s. Its head office is located in Meylan, near Grenoble (France), Kayentis is also present in Boston (USA).

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!

For more information about Kayentis, visit our career page, or have a look at our employee satisfaction survey results.

The Clinical Project Manager permanent position is based in Boston, MA.

The Clinical Project Manager manages clinical trials during their running and closing phases. For this purpose, you provide functional support to sponsor and site clinical teams as well as activity and data monitoring.

YOUR MISSION:
• You manage the activation of sites through accounts creation, shipment of devices, planning of trainings
• You pilot the resolution of the actions to be carried out on running projects and provide feedback during regular points with the sponsor or through the channels set up with the users
• You maintain regular contacts with the client (meetings & calls)
• You interact with the outsourced helpdesk
• You relay customer needs to internal teams
• You proactively monitor the key elements of the study and associated risks, and anticipate the key actions to be launched with the client in the running phase
• You manage communication & coordination of issues until resolution
• You manage the closing of sites through return of devices, shipment of archives

YOUR PROFILE:
• Bachelors or Masters degree in Life Science, Clinical Trials, Clinical Project Management, Clinical Research Associate with project management experience, or equivalent
• Minimum of 2 years in the field of clinical trials
• You demonstrate a sense of organization
• You are proactive and know how to organize your activities and manage priorities in an autonomous way with a resistance to pressure
• You have an excellent relationship, team spirit
• You are customer oriented with a good communication

YOUR BENEFITS:
• Flexible working hours
• Bonus
• Generous # of PTOs
• Health, Dental, Vision program
• 401K
• Commuters benefit

Are you interested in this opportunity? >> Contact us and send us your CV at *** <<

Qualifications

  • Bachelors or Masters degree in Life Science, Clinical Trials, Clinical Project Management, Clinical Research Associate with project management experience, or equivalent
  • Minimum of 2 years in the field of clinical trials
  • You demonstrate a sense of organization
  • You are proactive and know how to organize your activities and manage priorities in an autonomous way with a resistance to pressure
  • You have an excellent relationship, team spirit
  • You are customer oriented with a good communication

Benefits

  • Flexible working hours
  • Bonus
  • Generous # of PTOs
  • Health, Dental, Vision program
  • 401K
  • Commuters benefit

Responsibilities

  • The Clinical Project Manager manages clinical trials during their running and closing phases
  • For this purpose, you provide functional support to sponsor and site clinical teams as well as activity and data monitoring
  • You manage the activation of sites through accounts creation, shipment of devices, planning of trainings
  • You pilot the resolution of the actions to be carried out on running projects and provide feedback during regular points with the sponsor or through the channels set up with the users
  • You maintain regular contacts with the client (meetings & calls)
  • You interact with the outsourced helpdesk
  • You relay customer needs to internal teams
  • You proactively monitor the key elements of the study and associated risks, and anticipate the key actions to be launched with the client in the running phase
  • You manage communication & coordination of issues until resolution
  • You manage the closing of sites through return of devices, shipment of archives


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