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Cra I/ Ii

Thermo Fisher Scientific
Thermo Fisher Scientific
1-1.6 years
Not Disclosed
10 Jan. 20, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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 Research Associate (CRA I / II) – Clinical Trials

Company: Thermo Fisher Scientific – PPD Clinical Research Services
Location: Mumbai, Maharashtra, India
Job Type: Full-Time
Category: Clinical Research / Monitoring
Experience Required: 1–1.5 Years On-site Clinical Trial Monitoring


Job Overview

Thermo Fisher Scientific’s PPD Clinical Research Services is seeking Clinical Research Associates (CRA I / II) to join our global clinical trials team. This role offers the opportunity to coordinate and oversee clinical study activities from start-up through close-out for assigned investigational sites. You will contribute to high-quality clinical research supporting life-changing therapies across therapeutic areas.

As a CRA, you will perform remote and on-site monitoring, ensure compliance with ICH-GCP and SOPs, maintain audit readiness, and build strong collaborative relationships with study sites and internal project teams. You will also mentor and guide junior colleagues where applicable.


Key Responsibilities

Clinical Site Monitoring

  • Conduct on-site monitoring visits per client SOPs and project-specific requirements

  • Perform risk-based monitoring, source data verification, and source document review

  • Collaborate with clinical sites to resolve issues, ensure protocol compliance, and maintain study integrity

  • Support country metrics tracking and study progress reporting

Documentation & Compliance

  • Prepare and submit accurate monitoring reports and follow-up letters

  • Ensure adherence to GCP, ICH guidelines, and applicable regulatory requirements

  • Support site audits/inspections and CAPA implementation

  • Maintain timely completion of administrative tasks, including expense reports and timesheets

Project & Client Management

  • Serve as a primary point of contact for assigned clinical trials

  • Collaborate with internal project teams, clients, and investigative sites to achieve clinical goals and timelines

  • Take ownership of identified risks/issues and ensure successful resolution

  • Participate in client meetings, study progress updates, and continuous improvement initiatives

Travel

  • Up to 60–75% travel to clinical sites may be required


Educational & Experience Requirements

Education

  • Postgraduate degree in Life Sciences or related field

Experience

  • 1–1.5 years of on-site monitoring experience in clinical trials (mandatory)

  • Demonstrated knowledge of ICH-GCP guidelines and regulatory requirements

  • Experience working in a Functional Service Provider (FSP) model preferred but not mandatory

  • Valid driver’s license where applicable

Skills & Competencies

  • Strong client relationship management skills

  • Proficiency in clinical research processes, medical terminology, and SOP interpretation

  • Attention to detail and accurate record-keeping

  • Excellent verbal and written communication skills

  • Ability to work independently and in a team environment

  • Digital literacy, including CTMS, EDC, IWRS, eTMF systems, and Microsoft Office

  • Ability to manage multiple projects simultaneously and prioritize effectively

  • Knowledge of RBQM concepts for risk-based site monitoring