CDA II

April 28, 2026 Auto Import

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Data Assoc II – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Clinical Data Assoc II, you will perform advanced aspects of the data cleaning process with a high level of accuracy and in accordance with Good Clinical Practices (GCPs) and Standard Operating Procedures/Work Process Documents (SOPs/WPDs), to assess the safety and efficacy of investigational products and/or medical devices. What You’ll Do: • Identify, resolve, and update data discrepancies. Make changes to the data management database as required. • Generate, track and resolve data clarifications and queries. May implement CRF design in identified graphic design package. • Review data listings for accuracy and consistency of data. Analyze and resolve data validation and other data management reports. • Produce project-specific status reports for CDM management and for clients on a regular basis. • Perform data management activities such as Serious Adverse Event and Third Party Vendor reconciliations as well as Data Listing reviews. Education and Experience Requirements: • Any Life Science Graduate • Technical positions may require a certificate • 4-6 Years of experience in Clinical Data Manager RoleHaving Experience in Veeva EDC is preferred. Knowledge, Skills and Abilities: • Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations • Strong attention to detail and skill with numbers and ability to use interactive computer programs • Good written and verbal communication skills and a strong command of English language and grammar • Good organizational and analytical/problem-solving skills • Ability to work productively with moderate supervision • Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data • Strong customer focus and excellent interpersonal skills. • Proven flexibility, adaptability and ability to work in a team environment or independently as needed • Must demonstrate good judgment in making decisions • Knowledge of medical/clinical trial terminology • Understands project protocol and Data Validation Manual Working Conditions and Environment: • Work is performed in an office or clinical environment with exposure to electrical office equipment. • Occasional drives to site locations. Potential Occasional travel required. Why Join Us? When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference. Apply today to help us deliver tomorrow’s breakthroughs.

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