Senior Clinical Data Associate

**Work Schedule** Second Shift (Afternoons) **Environmental Conditions** Office **Job Description** Join Us as a **Senior Clinical Data Associate** – 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 Senior Clinical Data Associate, you will perform all aspects of the data cleaning process, with minimal supervision, in accordance with Good Clinical Practices (GCP) 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: * Supports the setup of study activities such as database design, testing of data entry screens, and Data Validation Manual (DVM) creation, as required. * Reviews data listings for accuracy and consistency of data. * Acts as point person and subject matter expert for specialized study-specific processes. * Generates, tracks and resolves data clarifications and queries and makes changes to the clinical database (EDC) as required. * Contributes to the improvement of data management processes on a global level. * Produces project-specific status reports for management and/or clients on a regular basis. * Provides training and work direction to junior staff as required. Education and Experience Requirements: * **Bachelor’s degree or equivalent, with relevant formal academic or vocational qualifications.** * **Prior experience in clinical research, including hands-on experience managing and handling clinical data, is required.** 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 • Good written and verbal communication skills • Good analytical/problem-solving skills • 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 and adaptability • Must be able to set and meet timelines or be able to negotiate schedule changes in response to project demands • Knowledge of medical/clinical terminology • Understands project protocol and DVM • Proven ability in achieving applicable technical competencies per the DM competency grid Working Conditions and Environment: * Work is performed in an office environment with exposure to electrical office equipment. * Hybrid Work Arrangement (2x a week in the office) * Occasional drives to site locations 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.