Clinical Data Manager

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.