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Clinical Project Manager

  • Full Time, onsite
  • Voisin Consulting Life Sciences (VCLS)
  • Cambridge, United States of America
Salary undisclosed

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Clinical Project Manager

We're looking for a Clinical Project Manager (CPM) to lead the execution of clinical trials from start-up through closeout. You'll be the driving force ensuring studies are delivered on time, within budget, and in compliance with all regulatory and quality standards.

What You'll Do:

  • Manage all phases of clinical trials, ensuring adherence to scope, timelines, and quality standards
  • Lead cross-functional teams and collaborate with sponsors, investigators, and vendors
  • Oversee study documentation, protocol development, and regulatory submissions
  • Monitor budgets, timelines, and site performance
  • Identify and mitigate risks, escalate deviations, and support audits
  • Contribute to proposals, bid defences, and contract negotiations
  • Mentor junior team members and support process improvements




Requirements

  • Proven experience managing clinical trials end-to-end
  • Deep understanding of GCP, ICH guidelines, and regulatory requirements
  • Strong leadership, problem-solving, and communication skills
  • Experience with vendor and budget management

Clinical Project Manager

We're looking for a Clinical Project Manager (CPM) to lead the execution of clinical trials from start-up through closeout. You'll be the driving force ensuring studies are delivered on time, within budget, and in compliance with all regulatory and quality standards.

What You'll Do:

  • Manage all phases of clinical trials, ensuring adherence to scope, timelines, and quality standards
  • Lead cross-functional teams and collaborate with sponsors, investigators, and vendors
  • Oversee study documentation, protocol development, and regulatory submissions
  • Monitor budgets, timelines, and site performance
  • Identify and mitigate risks, escalate deviations, and support audits
  • Contribute to proposals, bid defences, and contract negotiations
  • Mentor junior team members and support process improvements




Requirements

  • Proven experience managing clinical trials end-to-end
  • Deep understanding of GCP, ICH guidelines, and regulatory requirements
  • Strong leadership, problem-solving, and communication skills
  • Experience with vendor and budget management