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Costa Rica
Hybrid
At Clario, a part of Thermo Fisher Scientific, we are transforming lives by delivering industry-leading clinical evidence that advances patient care. As a Clinical Data Manager, you will play a critical role in ensuring the quality, integrity, and accuracy of imaging clinical trial data across a variety of therapeutic areas. This position offers the opportunity to collaborate with global study teams, contribute to innovative clinical research, and help bring life-changing therapies to patients worldwide.
What We Offer
Competitive compensation
Private medical and dental insurance
Life insurance coverage
Annual bonus (Aguinaldo) and vacation in accordance with Costa Rican labor law
Flexible and hybrid work options
Wellness and learning programs
What You'll Be Doing
Perform all clinical data management deliverables for assigned clinical studies.
Participate in client meetings and provide data management expertise and support.
Understand study implementation requirements and clinical data collection processes.
Collaborate with cross-functional project teams to develop study-specific edit check criteria.
Define, execute, review, and maintain edit checks while resolving data discrepancies.
Maintain accurate, complete, and current study documentation.
Support study setup activities including database structure, specifications, testing, and approvals.
Coordinate, document, and manage the receipt and processing of electronic and ancillary data from external sources, including sponsors, CROs, and laboratories.
Monitor study progress and communicate project status updates to management.
Review clinical data to identify inconsistencies, errors, and quality concerns.
Partner with project teams to investigate and resolve data issues in a timely manner.
Track outstanding discrepancies and ensure appropriate follow-up through resolution.
Ensure all clinical data management activities comply with applicable regulatory requirements and company standards.
Adhere to departmental procedures, policies, work instructions, and Standard Operating Procedures (SOPs).
Contribute to the development and continuous improvement of departmental standards and processes.
Participate in the review and maintenance of data management-related SOPs.
Support team objectives through collaboration, knowledge sharing, and continuous improvement initiatives.
Maintain technical and industry knowledge through ongoing professional development and company-sponsored training.
What We Look For
Bachelor's degree in Computer Science, Life Sciences, or a related field, or equivalent combination of education and experience.
Minimum of 1 year of experience in a clinical data management, pharmaceutical, biotechnology, or contract research organization (CRO) environment.
Working knowledge of relational databases, data validation principles, and database management processes.
Experience reviewing, cleaning, and validating clinical trial data.
Familiarity with SAS is preferred.
Proficiency with Microsoft Office applications, including Excel, Word, and Access.
Understanding of clinical trial processes, terminology, and regulatory expectations.
Strong analytical, problem-solving, and organizational skills.
Excellent written and verbal communication skills.
Ability to work independently and effectively within a collaborative team environment.
Exceptional attention to detail and commitment to quality.
Ability to manage competing priorities in a dynamic, deadline-driven environment.
Ability to maintain a professional, positive, and customer-focused approach.
At Clario, a 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.
