Senior Clin Data Assoc

**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** 🌟 Senior Clinical Data Associate ================================= ### 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) * Standard Operating Procedures / Work Process Documents (SOPs/WPDs) Your work will support the assessment of the safety and efficacy of investigational products and/or medical devices. 🔹 What You’ll Do ================= ### 📊 Clinical Data Management Activities * Support the setup of study activities such as: * Database design * Testing of data entry screens * Data Validation Manual (DVM) creation as required * Review data listings for accuracy and consistency * Generate, track, and resolve data clarifications and queries * Make changes to the clinical database as required ### 🧠 Subject Matter Expertise & Process Improvement * Act as point person and subject matter expert for specialized study-specific processes * Contribute to the improvement of data management processes on a global level * Understand project protocol and DVM requirements ### 📈 Reporting & Collaboration * Produce project-specific status reports for management and/or clients on a regular basis * Provide training and work direction to junior staff as required * Collaborate with project teams while maintaining high quality standards 🎓 Education & Experience Requirements ====================================== ### Required: * Bachelor’s degree or equivalent and relevant formal academic/vocational qualification ### Experience: * Previous experience that provides the knowledge, skills, and abilities to perform the job comparable to 0 to 2 years 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. 🧠 Knowledge, Skills & Abilities ================================ ✅ Ability to apply knowledge and skills in a highly organized fashion while adhering to: * Regulatory guidelines * Global SOPs * Client expectations ✅ Strong attention to detail and numerical skills ✅ Good written and verbal communication skills ✅ Good analytical and problem-solving skills ✅ Ability to maintain a high degree of confidentiality with clinical and proprietary client data ✅ Strong customer focus and excellent interpersonal skills ✅ Proven flexibility and adaptability ✅ Ability to set and meet timelines or negotiate schedule changes in response to project demands ✅ Knowledge of medical/clinical terminology ✅ Proven ability in achieving applicable technical competencies per the DM competency grid 🌍 Working Conditions & Environment =================================== * Work is performed in an office environment with exposure to electrical office equipment * Occasional drives to site locations * Occasional travel both domestic and international 🚀 Why Join Us? =============== When you join Thermo Fisher Scientific, you become part of a global team that values: * Passion * Innovation * 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.**