Clario

Clinical Project Manager

Clario Costa Rica

Biotechnology Research · 1,001-5,000 employees

Yesterday
Remote project-manager Mid (2-5 yrs) Full-time United States
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About the role

The Clinical Project Manager will lead cross-functional teams in the execution of clinical trials, overseeing study startup, project planning, and closeout activities. They are responsible for maintaining high standards of quality and compliance while managing project finances and resources.

What they look for

Clinical trials Project management Study startup Project planning Financial oversight Regulatory compliance GCP ICH FDA Team leadership Cross-functional collaboration Microsoft Word Microsoft Excel Microsoft Access Microsoft Project

Requirements

Candidates must possess a bachelor's degree in a life sciences or healthcare field and have 1–3 years of clinical trials experience. Proficiency in project management tools and a strong understanding of regulatory guidelines such as GCP, ICH, and FDA are required.

Benefits

Medical coverage Dental coverage Vision coverage Flexible time off Paid time off Tuition reimbursement Employee assistance program Wellness programs

Full description

Job Description

At Clario, part of Thermo Fisher Scientific is seeking a Clinical Project Manager to lead cross-functional teams in the execution of clinical trials. This role is pivotal in ensuring timely delivery of study startup, project execution, and closeout activities while maintaining high standards of quality and compliance. You’ll collaborate with internal departments and external stakeholders to drive project success and contribute to Clario’s mission of unlocking better evidence for life-changing therapies.

What We Offer

  • Competitive compensation
  • Medical, dental, and vision coverage
  • Flexible and paid time off
  • Remote and hybrid work options
  • Tuition reimbursement
  • Employee assistance and wellness programs

 

What You’ll Be Doing

  • Lead study startup activities by reviewing protocol requirements, defining project plans, and coordinating documentation with stakeholders
  • Manage project execution through resource planning, financial oversight, and adherence to SOPs and regulatory guidelines
  • Provide team leadership by setting performance expectations, delivering training, and supporting coaching and mentoring efforts
  • Support business development by contributing to capability presentations and representing Clario at professional meetings
  • Oversee project closeout by coordinating submission activities and ensuring completion of all final deliverables

 

What We Look For

  • Bachelor’s degree in life sciences, pharmacy, nursing, or related healthcare field, or equivalent experience
  • 1–3 years of clinical trials experience within a CRO or pharmaceutical research organization, preferably in project management
  • Proven expertise in project planning, financial tracking, and regulatory compliance (GCP, ICH, FDA)
  • Strong proficiency in Microsoft Word, Excel, Access, and Project
  • Demonstrated ability in leadership, communication, and cross-functional collaboration

 

At Clario, part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

At Clario, part of Thermo Fisher Scientific is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

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