Assistant Clinical Project Manager
Clario San José, San José, Costa Rica
Biotechnology Research · 1,001-5,000 employees
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About the role
The Assistant Clinical Project Manager supports the execution of global clinical studies by drafting documentation, monitoring data flow, and liaising with cross-functional teams. They also act as a point of contact for clients, ensure protocol compliance, and assist in resolving project-related issues.
What they look for
Requirements
Candidates must hold a Bachelor's degree and have at least one year of experience in pharmaceutical drug development or clinical research. Proficiency in Microsoft Office and strong organizational and communication skills are required for this role.
Benefits
Full description
Clario, part of Thermo Fisher Scientific, is seeking a detail‑oriented Assistant Clinical Project Manager to support the successful execution of global clinical studies. In this role, you will work closely with Clinical Project Managers and cross‑functional teams to ensure high‑quality, timely delivery of clinical projects in a regulated environment. This position offers an excellent opportunity to build hands‑on experience in clinical research while contributing to our mission of transforming lives through better evidence.
What We Offer
- Competitive compensation
- Private health insurance
- Engaging employee programs
- Flexible work schedules
- Attractive PTO plan
- Flex workspace
What You’ll Be Doing
- Support Clinical Project Managers in drafting project documentation and reviewing presentations
- Participate in project meetings, training sessions, and client calls
- Read and interpret clinical protocol documents
- Liaise with cross-functional teams to ensure timely delivery of study milestones
- Monitor internal data flow and task completion within agreed timelines
- Respond to inquiries professionally and promptly
- Communicate project status updates to clients
- Verify imaging protocol compliance and manage related queries
- Act as Project Manager when assigned PM is unavailable
- Mentor and support Operations team members; provide feedback to Operations Manager
- Follow up on outstanding items such as missing data or incomplete documentation
- Assist in resolving client issues and serve as an additional point of contact
- Adhere to Standard Operating Procedures (SOPs) and regulatory guidelines (GCP, ICH, FDA)
- Contribute to SOP and process document updates and operational improvements
What We Look For
Education:
- Bachelor’s degree required
Experience:
- 1 plus years of experience working in pharmaceutical drug development, clinical trials, and/or clinical research preferred
- Healthcare, medical experience, and/or clinical research, preferred
- Proficiency in Microsoft Office tools
- Ability to work independently and collaboratively in a fast-paced environment
- Strong attention to detail and organizational skills
- Excellent verbal and written communication skills
- Professional and positive attitude
- Availability to work in a hybrid model from San Jose
- Travel requirement: 0–5%
At Clario, 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.
Clario 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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