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.