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Clin Data Assoc Ii

Thermo Fisher Scientific
Thermo Fisher Scientific
1.6-3 years
preferred by company
10 Jan. 9, 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

Clinical Data Associate II (CDA II) – Remote, India

Job ID: R-01338260
Job Type: Full-Time
Category: Clinical Research / Clinical Data Management
Work Mode: Fully Remote
Location: India

About the Role

Join Thermo Fisher Scientific’s Clinical Research Services team as a Clinical Data Associate II and play a key role in ensuring the integrity, accuracy, and timeliness of clinical trial data. This position offers the opportunity to work with global data management teams supporting top pharmaceutical and biotechnology sponsors across multiple therapeutic areas. You will contribute to advanced data review, query resolution, and database management while supporting study start-up, ongoing trials, and inspection readiness.

As part of the Functional Service Provider (FSP) model, you will collaborate with cross-functional stakeholders, produce high-quality datasets, and ensure data integrity in compliance with ICH-GCP guidelines, SOPs, and regulatory requirements.

Key Responsibilities

  • Perform advanced data review, cleaning, and reconciliation activities to ensure high-quality, analysis-ready datasets

  • Manage and resolve complex data queries, discrepancies, and updates within the clinical data management system (Medidata RAVE / Veeva EDC)

  • Conduct SAE and third-party vendor reconciliations, as well as review data listings and validation reports

  • Implement CRF design updates and contribute to database modifications as required

  • Produce accurate project-specific status reports for stakeholders, CDM management, and clients

  • Collaborate with cross-functional teams to proactively identify and mitigate risks or data issues

  • Ensure adherence to regulatory and sponsor-specific guidelines, SOPs, and quality standards

  • Support audit readiness and inspection preparedness

Education & Experience Requirements

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field

  • 1.6 – 3 years of relevant experience in Clinical Data Management or a CRO/FSP environment

  • Hands-on experience with RAVE or Veeva EDC systems

Knowledge, Skills & Competencies

  • Strong understanding of medical and clinical trial terminology

  • Ability to interpret study protocols and follow Data Validation Manuals

  • Excellent analytical and problem-solving skills with strong attention to detail

  • Proficient in interactive computer programs and database systems

  • Strong written and verbal communication skills with command of English grammar

  • Ability to work independently and collaboratively in a team environment

  • High degree of confidentiality, integrity, and ethical responsibility in handling clinical data

  • Flexibility and adaptability to changing project needs and timelines

  • Strong customer focus and interpersonal skills

Working Conditions

  • Office-based or remote clinical environment with standard office equipment

  • Occasional travel to study sites may be required

Career Growth Opportunities

Thermo Fisher Scientific’s FSP model offers structured learning pathways, mentorship, and exposure to global clinical trials. CDA II professionals can progress along the Clinical Data Management career ladder:

  • Senior Clinical Data Associate → Clinical Data Team Lead → Clinical Data Manager → CDM Project Manager

  • Opportunities to transition into Data Standards or Programming roles based on skill, business need, and impact

Why Join Us

  • Gain global exposure across international clinical trials, CROs, vendors, and sponsor teams

  • Take end-to-end ownership of study data management activities from start-up through database lock

  • Strengthen analytical, project management, and risk management skills

  • Work with AI-enabled tools and modern EDC platforms to enhance data quality and clinical insights

  • Be part of a team that delivers life-changing medicines to patients worldwide

About Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in serving science, generating annual revenues exceeding $44 billion. Through its PPD® Clinical Research Services, the company accelerates the development of new therapies, supports clinical operations globally, and empowers scientific innovation. Thermo Fisher employs over 90,000 colleagues across the world and is committed to fostering a diverse, inclusive, and equal opportunity work environment.

For more information, visit www.thermofisher.com.