About this role
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.