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Clin Data Assoc Ii

Thermo Fisher Scientific
Thermo Fisher Scientific
1.6-3 years
preferred by company
10 Jan. 20, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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 (CDA II)
Location: Remote – India
Employment Type: Full-Time
Work Model: Fully Remote
Experience Required: 1.6–3 Years
Industry: Clinical Research | Clinical Data Management
Job ID: R-01338260


About the Role

Thermo Fisher Scientific is hiring a Clinical Data Associate II to support global clinical trials within its PPD® Clinical Research Services portfolio. This role is ideal for professionals with hands-on experience in clinical data review, reconciliation, and EDC systems who are ready to take ownership of complex data management activities in a fast-paced, regulated environment.

As a CDA II, you will play a critical role in ensuring data accuracy, integrity, and inspection readiness across studies conducted for leading pharmaceutical and biotechnology organizations worldwide.


Key Responsibilities

  • Perform advanced clinical data cleaning, review, and reconciliation activities in compliance with ICH-GCP, global SOPs, and study protocols

  • Identify, analyze, and resolve complex data discrepancies and queries within EDC systems

  • Generate, track, and close data clarification forms (DCFs) and manage query lifecycles

  • Review data listings, validation outputs, and data management reports for accuracy and consistency

  • Perform SAE reconciliations and third-party vendor data reconciliations

  • Support CRF design updates and database changes using approved tools

  • Prepare and deliver project-specific data status and metrics reports for internal stakeholders and clients

  • Collaborate closely with cross-functional teams to proactively manage risks and data quality issues


Education & Experience

  • Bachelor’s degree or equivalent in Life Sciences, Pharmacy, Clinical Research, or a related discipline

  • 1.6 to 3 years of relevant experience in clinical data management or clinical research

  • Mandatory hands-on experience with RAVE and/or Veeva EDC platforms


Required Skills & Competencies

  • Strong knowledge of clinical trial processes, medical terminology, and data validation principles

  • High attention to detail with strong analytical and problem-solving abilities

  • Proficiency in handling interactive clinical data management systems

  • Excellent written and verbal communication skills with strong command of English

  • Ability to work effectively with moderate supervision in a remote, global team environment

  • Strong organizational skills with a customer-focused mindset

  • Proven ability to maintain confidentiality of clinical and proprietary data

  • Good judgment and decision-making capabilities

  • Working understanding of study protocols and Data Validation Manuals


Working Conditions

  • Remote office-based role with standard working hours (Monday to Friday)

  • Occasional travel to clinical sites may be required, based on study needs


Career Growth & Development

You will be part of a dedicated FSP (Functional Service Provider) model, supporting a globally recognized biopharmaceutical sponsor with a strong legacy in specialty medicines, vaccines, and scientific innovation. This role offers:

  • Exposure to global, multi-phase clinical trials across therapeutic areas

  • Collaboration with international data science, clinical, and regulatory teams

  • Structured learning paths, mentorship, and stretch assignments

  • Clear career progression opportunities into Senior CDM, CDTL, CDM Project Management, or Data Standards and Programming roles


Why Join Thermo Fisher Scientific?

  • Contribute to life-changing therapies that impact patients worldwide

  • Gain hands-on experience with modern Clinical Data Management tools, including AI-enabled workflows

  • Work in a mature global delivery model focused on quality, partnership, and innovation

  • Be part of a mission-driven organization committed to scientific excellence


About Thermo Fisher Scientific

Thermo Fisher Scientific Inc. is a global leader in serving science, with annual revenue exceeding $44 billion. With more than 90,000 colleagues worldwide, the company supports customers across life sciences research, clinical development, diagnostics, and pharmaceutical manufacturing through industry-leading brands such as Thermo Scientific, PPD, Patheon, Invitrogen, and Fisher Scientific.

Thermo Fisher Scientific is an Equal Employment Opportunity Employer and is committed to fostering an inclusive and diverse workforce.