Clinical Research Job at Thermo Fisher Scientific | Apply Now
Thermo Fisher Scientific is inviting applications for the Clinical Data Associate I (CDA I) position. This clinical research job is a fully remote role based in India, supporting a high-profile Functional Service Provider (FSP) client—a leading global biopharmaceutical organization. As a CDA I, you will play a foundational role in ensuring the integrity of clinical trial data by performing data cleaning and reconciliation in accordance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs). This is an entry-level opportunity within the thermo fisher career track, offering a pathway into modern Clinical Data Management (CDM) and AI-enabled workflows.
- Job Position: Clinical Data Associate
- Job ID: R-01338259.
- Location: Fully Remote, India.
- Category: Clinical Research.
About the Company
Thermo Fisher Scientific is the world leader in serving science, with annual revenues exceeding $44 billion. The company’s Mission is to enable customers to make the world healthier, cleaner, and safer. Through its industry-leading brands—including Thermo Scientific, Applied Biosystems, and PPD (the clinical research business)—it supports the global pharmaceutical and biotech industries in accelerating research and improving patient therapies.
Job Overview
The CDA I is responsible for high-accuracy data entry, cleaning, and reconciliation activities. You will work within Electronic Data Capture (EDC) systems, specifically Medidata Rave and Veeva Vault, to ensure that clinical study data is accurate, consistent, and inspection-ready.
Requirements & Qualifications
To be eligible for this clinical research job, candidates must meet the following criteria:
- Education: Bachelor’s degree or equivalent formal academic qualification in a relevant field.
- Experience: Minimum 1 to 1.6 years of experience in clinical data management or a related area.
- Technical Skills: Mandatory experience in RAVE or Veeva EDC systems.
- Knowledge: Familiarity with GCP (Good Clinical Practice), SOPs, and project protocols/Data Validation Manuals (DVM).
Key Responsibilities
- Data Discrepancy Management: Identify, resolve, and update discrepancies within the data management database.
- Query Resolution: Generate, track, and resolve data clarifications and queries to ensure data quality.
- Collaboration: Partner with cross-functional study teams to maintain data integrity throughout the study lifecycle.
- Design Support: May assist with Case Report Form (CRF) design using identified graphic design packages.
Applying for the Clinical Data Associate I role is an excellent move for professionals looking to establish a long-term thermo fisher career in the evolving landscape of data-driven clinical trials. This clinical research job provides the stability of a global leader combined with the innovation of AI-supported data management. If you have 1+ years of experience in EDC systems and a commitment to data quality, apply today to help bring life-changing medicines to patients worldwide.
