Sr Clinical Data Associate

Work Schedule Standard (Mon-Fri)

Environmental Conditions Office

🌟 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.