Thermofisher Hiring for Clinical Data Associate II Role
ThermoFisher Scientific, a global leader in clinical research services and life sciences solutions, is hiring for the role of Clinical Data Associate II on a remote basis. This opportunity is suitable for experienced professionals with 1.6 to 3 years of experience in Clinical Data Management (CDM) who are looking to grow their career in a global clinical research environment.
The role focuses on supporting clinical data review, discrepancy management, query resolution, data reconciliation, and database quality activities across clinical studies. Candidates will work closely with data managers, project teams, and cross‑functional stakeholders to ensure accurate, compliant, and timely clinical trial data delivery.
🏢 About the Employer
Thermo Fisher Scientific is a global leader in life sciences research, clinical development, and laboratory services. The organization supports pharmaceutical and biotechnology companies across the clinical trial lifecycle, operating under strict regulatory and quality standards. Professionals at Thermo Fisher gain exposure to global clinical studies, advanced data platforms, and compliance‑driven environments.
📊 Job Summary
- Position: Clinical Data Associate II
- Department: Clinical Research
- Location: Remote
- Experience: 1.6 – 3 Years
- Qualification: B.Pharm, M. Pharm
- Job Type: Full-Time
- Last Date to apply: 31 March 2026
📋 Key Duties – Clinical Data Associate II
- Identify, resolve, and update data discrepancies and make required updates within the clinical data management database.
- Generate, track, and resolve data queries and clarifications efficiently.
- Support CRF design implementation using approved graphical design tools when required.
- Review data listings to ensure accuracy, completeness, and consistency.
- Analyze and resolve issues identified through data validation checks and data management reports.
- Prepare and deliver project‑specific status reports for CDM management and clients on a regular basis.
- Perform key data management tasks, including Serious Adverse Event (SAE) reconciliation, third‑party vendor reconciliation, and data listing reviews, ensuring data integrity and regulatory compliance..
🎓 Eligibility Requirements
- Bachelor’s degree or equivalent relevant formal academic qualification.
- 1.6 to 3 years of professional experience in Clinical Data Management (CDM) or a related role, providing the required knowledge and skills to perform the job.
- Hands‑on experience working with Medidata RAVE and/or Veeva EDC systems is required.
- Apply data management knowledge in an organized and structured manner, adhering to global SOPs, regulatory guidelines, and client expectations.
🧠 Core Skills
- Strong attention to detail with good numerical skills and the ability to work confidently with interactive clinical data systems.
- Good written and verbal communication skills, with strong command of the English language and grammar.
- Effective organizational, analytical, and problem‑solving abilities to manage data review and resolution activities.
⭐ Job Overview
The Clinical Data Associate II role plays a vital role in ensuring the accuracy, integrity, and reliability of clinical trial data. Professionals in this role bridge the gap between raw clinical data and final analysis datasets. Working at Thermo Fisher Scientific provides exposure to global trials, advanced EDC platforms, and robust quality systems, making this role a strong stepping stone toward senior CDM positions.
🎯 Best Fit Candidates
This opportunity is suitable for:
- Clinical Data Associates with 1.6–3 years of experience
- Professionals experienced with Medidata RAVE or Veeva EDC
- Candidates seeking growth in global CDM operations
- Individuals comfortable working in regulated, SOP‑driven environments
📈 Future Growth
With experience and consistent performance, professionals can progress into roles such as:
- Senior Clinical Data Associate
- Clinical Data Analyst
- Clinical Data Lead
- Data Quality or Project Coordination roles
Thermo Fisher Scientific supports career growth through structured learning and global exposure.
💰 Salary Details & Work Model
- Expected Salary: As per Thermo Fisher Scientific company standards
- Work model: Remote
💡 Professional Tips
- Highlight SOP compliance and regulatory experience in your resume
- Revise clinical data management concepts and workflows
- Strengthen hands‑on knowledge of Medidata RAVE or Veeva EDC
- Be prepared to discuss data validation and discrepancy handling scenarios
🔗How to Apply
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer: This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.
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📚 Career Guide
Prepare with Clinical Data Management interview questions
FAQ– Clinical Data Associate II
1. Who can apply for the Clinical Data Associate II role at Thermo Fisher?
Candidates with a Bachelor’s degree and 1.6 to 3 years of experience in Clinical Data Management (CDM) are eligible to apply.
2. Is this role fully remote?
Yes. This position offers remote work flexibility, though occasional travel to site locations may be required depending on project needs.
3. What kind of experience is required?
Candidates should have hands‑on experience in clinical data review, query management, discrepancy resolution, and working with EDC systems such as Medidata RAVE or Veeva EDC.
4. What are the main responsibilities of this role?
You will identify and resolve data discrepancies, manage data queries, review data listings, perform SAE and vendor reconciliations, and support data validation and reporting activities.
5. Will I work on global clinical trials?
Yes. Thermo Fisher supports global clinical studies, and you will collaborate with international project teams and stakeholders.
6. Is knowledge of regulatory guidelines required?
Yes. A working understanding of GCP, ICH guidelines, and clinical trial standards is important for this role.
