Looking for exciting pharma jobs and clinical research opportunities? Clario, part of Thermo Fisher Scientific, is hiring an Assistant Clinical Project Manager in Costa Rica.
This opportunity is ideal for professionals seeking pharmaceutical careers, clinical trial management experience, and global project exposure.
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About the Company
Clario, a part of Thermo Fisher Scientific, is a globally recognized clinical research and healthcare technology organization dedicated to transforming lives through better evidence.
The company supports pharmaceutical, biotechnology, and medical device organizations by delivering innovative clinical trial solutions and advanced data management services.
With a strong commitment to quality, regulatory compliance, and scientific excellence, Clario operates in a highly regulated environment following international standards such as Good Clinical Practice (GCP), International Council for Harmonisation (ICH), and FDA regulations.
The organization continues to drive innovation in clinical research while offering employees opportunities for professional growth and global collaboration.
Job Details
- Company Name: Clario (Part of Thermo Fisher Scientific)
- Position: Assistant Clinical Project Manager
- Experience: 1+ years preferred
- Qualification: Bachelor’s Degree
- Location: Costa Rica (San Jose)
- Work Type: Hybrid
- Employment Type: Full-Time
- Travel Requirement: 0–5%
Job Description
Clario is seeking a motivated and detail-oriented professional to support the successful execution of global clinical studies.
The role involves collaborating with Clinical Project Managers, clients, and cross-functional teams to ensure projects are delivered on time and in compliance with regulatory requirements.
Assistant Clinical Project Manager
- Department: Clinical Operations / Clinical Project Management
- Market: Clinical Research & Pharmaceutical Development
- Role: Project Coordination and Clinical Study Support
- Experience: 1+ years preferred
- Education/Qualification: Bachelor’s Degree
Skills/Qualifications
- Bachelor’s degree in a relevant discipline
- Experience in pharmaceutical drug development preferred
- Clinical trials or clinical research experience preferred
- Healthcare industry knowledge preferred
- Strong Microsoft Office proficiency
- Excellent organizational abilities
- Strong attention to detail
- Effective written communication skills
- Effective verbal communication skills
- Ability to work independently
- Strong teamwork and collaboration skills
- Positive and professional attitude
- Knowledge of GCP guidelines
- Understanding of ICH regulations
- Familiarity with FDA compliance requirements
Key Responsibilities
- Support Clinical Project Managers with project documentation
- Review presentations and study-related materials
- Participate in client meetings and training sessions
- Interpret clinical protocol documentation
- Coordinate cross-functional project activities
- Monitor study milestones and timelines
- Communicate project updates to clients
- Manage protocol compliance inquiries
- Verify imaging protocol compliance
- Follow up on missing project data
- Assist with issue resolution activities
- Mentor operations team members
- Support process improvement initiatives
- Contribute to SOP updates
- Ensure regulatory compliance requirements
Benefits/Perks
- Competitive compensation package
- Private health insurance
- Flexible work schedules
- Attractive paid time off plan
- Flexible workspace options
- Global project exposure
- Continuous learning opportunities
- Professional development support
- Collaborative work culture
- Career growth opportunities
- International team environment
How to Apply
Interested candidates can apply directly through the official Clario careers portal.
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Applicants are encouraged to submit their applications as early as possible, as positions may be filled once suitable candidates are identified.
Apply today and take the next step in your clinical research and pharmaceutical career journey.
Why You Should Join
Clario offers an excellent platform for professionals looking to build a long-term career in clinical research and pharmaceutical development.
As part of Thermo Fisher Scientific, employees benefit from a culture focused on innovation, compliance, collaboration, and scientific excellence.
FAQs
Who is eligible to apply for the Assistant Clinical Project Manager position?
Candidates with a Bachelor’s degree and preferably at least one year of experience in clinical research, clinical trials, or pharmaceutical drug development are encouraged to apply.
Is prior clinical research experience required?
Clinical research or pharmaceutical industry experience is preferred but not always mandatory if candidates possess relevant skills and qualifications.
Is this a remote position?
The role follows a hybrid work model and requires availability to work from San Jose, Costa Rica.
What career growth opportunities are available?
Employees gain exposure to global clinical studies, project management responsibilities, cross-functional collaboration, and professional development opportunities within a leading healthcare organization.
