SENIOR CLINICAL DATA ASSOCIATE

<p style="text-align:left"><b>Work Schedule</b></p>Standard (Mon-Fri)<p style="text-align:inherit"></p><p style="text-align:left"><b>Environmental Conditions</b></p>Office<p style="text-align:inherit"></p><p style="text-align:left"><b><u>Job Description</u></b></p><p style="text-align:inherit"></p>Join Us as a Senior Clinical Data Associate – Make an Impact at the Forefront of Innovation<br/>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. <br/> <br/>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.<br/>What You’ll Do:<br/>• Supports the setup of study activities such as database design, testing of data entry screens, and Data Validation Manual (DVM) creation, as required. <br/>• Reviews data listings for accuracy and consistency of data. <br/>• Acts as point person and subject matter expert for specialized study-specific processes. <br/>• Generates, tracks and resolves data clarifications and queries and makes changes to the clinical database as required. <br/>• Contributes to the improvement of data management processes on a global level. <br/>• Produces project-specific status reports for management and/or clients on a regular basis. <br/>• Provides training and work direction to junior staff as required.<br/><br/>Education and Experience Requirements:<br/>• Bachelor's degree or equivalent and relevant formal academic / vocational qualification <br/>• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years). <br/>In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.<br/><br/>Knowledge, Skills and Abilities: <br/>• Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations <br/>• Strong attention to detail and skill with numbers <br/>• Good written and verbal communication skills <br/>• Good analytical/problem-solving skills <br/>• Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data <br/>• Strong customer focus and excellent interpersonal skills. <br/>• Proven flexibility and adaptability <br/>• Must be able to set and meet timelines or be able to negotiate schedule changes in response to project demands <br/>• Knowledge of medical/clinical terminology <br/>• Understands project protocol and DVM <br/>• Proven ability in achieving applicable technical competencies per the DM competency grid <br/><br/><br/>Working Conditions and Environment: <br/>• Work is performed in an office environment with exposure to electrical office equipment. <br/>• Occasional drives to site locations <br/>• Occasional travel both domestic and international.<br/><br/>Why Join Us?<br/><br/>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.<br/><br/>Apply today to help us deliver tomorrow’s breakthroughs.<p></p><p></p><p></p><p></p>