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Clin Data Assoc Ii

Thermo Fisher Scientific
Thermo Fisher Scientific
2-3 years
₹6 LPA – ₹10 LPA (Estimated)
Remote
10 March 11, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Data Associate II
Location: Remote, India
Company: Thermo Fisher Scientific
Employment Type: Full-time
Salary: ₹6 LPA – ₹10 LPA (Estimated)


Job Description

Thermo Fisher Scientific is hiring a Clinical Data Associate II to support clinical data management activities across global clinical trials. In this role, you will perform advanced data review and data cleaning activities to ensure data integrity, accuracy, and regulatory compliance.

You will collaborate with cross-functional teams to resolve data discrepancies, manage complex queries, and support the preparation of high-quality datasets used to evaluate the safety and effectiveness of investigational products.


Key Responsibilities

  • Identify, resolve, and update clinical data discrepancies in data management systems.

  • Generate, track, and resolve data queries and clarifications with study teams.

  • Review data listings and validation reports for accuracy and consistency.

  • Perform Serious Adverse Event (SAE) and third-party vendor data reconciliations.

  • Support Case Report Form (CRF) design and database updates when required.

  • Produce project status reports for Clinical Data Management (CDM) leadership and clients.

  • Analyze and resolve data validation reports and other data management outputs.


Required Qualifications

  • Bachelor’s degree or equivalent relevant education.

  • 1.6 – 3 years of experience in clinical data management or related roles.

  • Hands-on experience with RAVE or Veeva EDC systems.


Skills & Competencies

  • Strong understanding of clinical trial data management and medical terminology.

  • Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.

  • Excellent attention to detail and analytical skills.

  • Good written and verbal communication in English.

  • Ability to work independently and collaboratively with global teams.

  • Strong problem-solving and organizational skills.

  • Ability to maintain confidentiality of clinical and proprietary data.


Work Environment

  • Remote or office-based work environment.

  • Occasional travel to clinical sites may be required.

  • Regular collaboration with global teams and stakeholders.


Career Growth

This role provides exposure to international clinical trials and opportunities to advance within Clinical Data Management roles such as:

  • Senior Clinical Data Manager

  • Clinical Data Team Lead

  • Clinical Data Management Project Manager

  • Data Standards / Clinical Programming roles


About the Company

Thermo Fisher Scientific is a global leader in scientific services, supporting pharmaceutical and biotechnology companies in developing innovative therapies. Through its PPD® clinical research portfolio, the company helps bring life-changing medicines to patients across more than 100 countries worldwide.