Clinical Data Associate I (Remote – India)
Location: Remote, India
Employment Type: Full-Time
Experience Required: 1–2 years in Clinical Data Management / EDC
Job ID: R-01338259
Category: Clinical Research / Data Management
About the Role
Thermo Fisher Scientific, a global leader in serving science, is seeking a Clinical Data Associate I to join our FSP Data Management team. This role is integral to ensuring high-quality, accurate clinical trial data in support of biopharmaceutical research and life-changing medicines. You will work closely with cross-functional study teams to maintain data integrity, resolve queries, and ensure inspection-ready datasets across global clinical trials.
This position offers remote work in India with opportunities for career growth along the Clinical Data Management track, including roles such as Senior CDM, CDTL, or CDM Project Manager, as well as potential transition into Data Standards or Clinical Programming.
Key Responsibilities
Perform entry-level clinical data cleaning and reconciliation activities in accordance with GCP, SOPs/WPDs, and study protocols
Identify, resolve, and update data discrepancies in clinical databases
Generate, track, and resolve data clarifications and queries
Implement CRF designs in designated EDC or graphic design platforms, as required
Support data quality and inspection readiness for clinical trials across multiple therapeutic areas
Collaborate with cross-functional teams including CRAs, study managers, and data management colleagues
Ensure confidentiality of clinical and proprietary data at all times
Required Qualifications & Experience
Bachelor’s degree or equivalent in Life Sciences, Pharmacy, or a related field
1–2 years of experience in clinical data management or clinical research, preferably with exposure to EDC systems such as RAVE or Veeva
Knowledge of clinical trial protocols, Data Validation Manuals, and global data standards
Skills & Competencies
Strong attention to detail and numerical accuracy
Excellent analytical, problem-solving, and organizational skills
Proficiency in EDC systems and ability to learn new clinical trial technologies
Good written and verbal communication skills with strong command of English
Ability to work independently while collaborating effectively with team members
Understanding of project protocols, SOPs, and regulatory compliance
Flexibility and adaptability to evolving study requirements
Career Growth & Opportunities
Global Exposure: Work on international clinical studies across multiple phases and therapeutic areas, partnering with CROs, vendors, and global teams
End-to-End Ownership: Contribute to the clinical study lifecycle, from set-up to close-out, enhancing operational and data management expertise
Learning & Development: Access structured mentorship, stretch assignments, and tailored learning pathways to advance along the CDM career track or transition into programming/data standards roles
Innovative Environment: Gain experience with AI-enabled workflows, advanced EDC platforms, and data-driven clinical trial delivery
About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in science, with annual revenue exceeding $44 billion and more than 90,000 employees worldwide. Our mission is to enable our customers to make the world healthier, cleaner, and safer through innovative technologies, laboratory services, and pharmaceutical solutions.
Website: www.thermofisher.com
Thermo Fisher Scientific is an Equal Opportunity Employer, committed to diversity and inclusion across its global operations.
Apply now on ThePharmaDaily.com to advance your career as a Clinical Data Associate with a leading global biopharmaceutical organization.
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