Thermo Fisher Hiring for Clinical Data Associate II: Pharma Jobs
Thermo Fisher Scientific is hiring experienced professionals for the role of Clinical Data Associate II, offering an excellent opportunity for candidates with prior hands‑on experience in clinical data management. In this role, you will contribute to high‑quality clinical trial data review, cleaning, and validation activities while working within global teams dedicated to advancing healthcare and scientific innovation.
This position is ideal for candidates who already have exposure to clinical data processes, CDMS tools, data validation checks, query management, and cross‑functional collaboration within clinical research settings. If you’re looking to advance your career in clinical data management with a world‑leading scientific organization, this opportunity at Thermo Fisher provides strong professional growth and learning potential.
Job Overview
- Position: Clinical Data Associate II
- Department: CDM
- Location: Remote
- Experience: 1.6 to 3 Years
- Qualification: B.Pharm, M.Pharm, BSc, MSc or equivalent
- Job Type: Full-Time
- Last date to apply: 01 March 2026
Key Responsibilities
- Identify & Resolve Data Discrepancies: Review clinical trial data to identify inconsistencies, resolve discrepancies, and update the clinical data management database as needed to maintain data integrity.
- Manage Data Queries & Clarifications: Generate, track, and resolve data clarifications and queries in a timely manner. You may also support CRF (Case Report Form) design using designated graphic design tools.
- Data Review & Quality Checks: Analyze data listings to ensure accuracy, completeness, and consistency across all clinical data fields. Address issues highlighted through data validation checks and system‑generated reports.
- Prepare Status Reports: Produce project‑specific data management status reports for CDM leadership and clients, providing regular updates on progress, outstanding items, and data quality metrics.
- Perform Core Data Management Activities: Conduct essential CDM tasks such as Serious Adverse Event (SAE) reconciliation, third‑party vendor data reconciliation, and detailed data listing reviews to ensure ongoing quality and compliance.
Required Skills & Qualifications
- Educational Background:
A Bachelor’s degree in a relevant field or an equivalent combination of formal academic education and practical experience that equips the candidate with the necessary clinical data management competencies. - Professional Experience:
1.6 to 3 years of prior experience in clinical data management or a closely related function, with proven ability to perform core CDM responsibilities such as data review, discrepancy management, query handling, and reconciliation activities. - EDC System Expertise:
Hands‑on experience with RAVE and/or Veeva EDC, including working within electronic data capture environments, managing CRFs, performing validation checks, and supporting database updates.
Preferred Skills & Experience (Good to Have)
Candidates with the following additional skills and experience will have an advantage:
- Regulatory & SOP Compliance: Applies clinical data management knowledge in a highly organized manner while strictly following regulatory guidelines, global SOPs, and specific client expectations.
- Strong Attention to Detail: Demonstrates exceptional accuracy, numerical aptitude, and the ability to work confidently with interactive computer systems and EDC platforms.
- Effective Communication: Possesses strong written and verbal English communication skills, with a solid command of grammar for clear documentation and professional interaction.
- Analytical & Problem‑Solving Ability: Shows strong organizational skills and the ability to identify, analyze, and resolve data‑related issues effectively.
- Independent & Guided Work Capability: Can work productively with moderate supervision while managing day‑to‑day tasks efficiently.
- Confidentiality & Data Integrity: Maintains a high level of confidentiality when handling clinical trial data and client‑proprietary information, ensuring data protection and compliance.
- Customer‑Focused & Collaborative: Exhibits excellent interpersonal skills, a strong customer service mindset, and the flexibility to work both independently and as part of a collaborative team.
- Sound Decision‑Making: Demonstrates good judgment and the ability to make informed decisions during routine and complex data management activities.
- Clinical Knowledge: Familiar with medical terminology, clinical trial processes, and essential CDM concepts.
- Protocol & DVM Understanding: Understands the study protocol and the Data Validation Manual (DVM), ensuring accurate and compliant data review and query handling.
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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