Thermofisher Hiring for Clinical Data Associate II Role

ByPharma Hiring Hub

Thermo Fisher 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.

This position offers remote work flexibility, exposure to global clinical trials, and strong career growth within Thermo Fisher’s clinical data management operations.

Thermo fisher cda 2 hiring

Job Overview

  • 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 Responsibilities – Clinical Data Associate II

  • Data Review & Discrepancy Management
  • Identify, resolve, and update data discrepancies and make required updates within the clinical data management database.
  • Query & Clarification Handling
  • Generate, track, and resolve data queries and clarifications efficiently.
  • Support CRF design implementation using approved graphical design tools when required.
  • Data Listing & Validation Review
  • Review data listings to ensure accuracy, completeness, and consistency.
  • Analyze and resolve issues identified through data validation checks and data management reports.
  • Study Status Reporting
  • Prepare and deliver project‑specific status reports for CDM management and clients on a regular basis.
  • Core CDM Activities
  • 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..

Required Skills & Qualifications

  • Educational Background: Bachelor’s degree or equivalent relevant formal academic qualification.
  • Experience Requirement: 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.
  • EDC System Experience: Hands‑on experience working with Medidata RAVE and/or Veeva EDC systems is required.
  • Regulatory & Process Compliance: Apply data management knowledge in an organized and structured manner, adhering to global SOPs, regulatory guidelines, and client expectations.
  • Attention to Detail & Accuracy: Strong attention to detail with good numerical skills and the ability to work confidently with interactive clinical data systems.
  • Communication Skills: Good written and verbal communication skills, with strong command of the English language and grammar.
  • Analytical & Problem‑Solving Skills: Effective organizational, analytical, and problem‑solving abilities to manage data review and resolution activities.

Why Join Thermofisher?

  • Global Life Sciences Leader
  • Be part of Thermo Fisher Scientific, a globally recognized organization supporting clinical research, diagnostics, and life sciences innovation across international markets.
  • Strong Career Path in Clinical Data Management
  • The Clinical Data Associate II role offers hands‑on exposure to data review, query management, reconciliation activities, and database quality control, helping you strengthen your career in Clinical Data Management.
  • Exposure to Global Clinical Trials
  • Work on international clinical studies, collaborating with data managers, project teams, and cross‑functional stakeholders to deliver high‑quality clinical trial data.
  • Remote Work Flexibility
  • Enjoy the benefit of remote working, providing work‑life balance while remaining actively engaged in global CDM operations.

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

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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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.

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