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Cra I/ Ii

Thermo Fisher Scientific
Thermo Fisher Scientific
1–1.5 years
Not Disclosed
10 Dec. 22, 2025
Job Description
Job Type: Full Time 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

Title: Clinical Research Associate (Level I / II) – Mumbai, Maharashtra, India
Location: Mumbai, Maharashtra, India
Job Type: Full-Time
Category: Clinical Research / FSP / Monitoring

Company Overview:
Join PPD® Clinical Research Services, part of Thermo Fisher Scientific, a leading global Contract Research Organization (CRO) supporting top pharmaceutical and biotech companies. With 2,700+ clinical trials conducted across 100+ countries over the last five years, we are at the forefront of drug development innovation, helping bring life-changing therapies to patients worldwide.

Role Overview:
We are seeking a Clinical Research Associate (CRA Level I/II) to coordinate and oversee all clinical aspects of assigned trials, from start-up to close-out. This role involves remote and on-site monitoring, risk-based site evaluation, and ensuring compliance with ICH-GCP, SOPs, and applicable regulations. You will develop collaborative relationships with clinical sites and clients, monitor trial progress, and contribute to continuous improvement in clinical processes.

Key Responsibilities:

  • Serve as a primary point of contact for assigned clinical trials and manage client relationships.

  • Conduct on-site monitoring visits, risk-based monitoring, source data verification (SDV), and source document reviews.

  • Work with client systems such as CTMS, EDC, IWRS, and eTMF to maintain study integrity.

  • Support in maintaining country metrics and ensuring audit readiness.

  • Collaborate with clinical sites to resolve issues, maintain compliance, and achieve project deliverables.

  • Prepare and submit monitoring reports, follow-up letters, and study documentation timely and accurately.

  • Support site audits/inspections and assist in the implementation of corrective and preventive actions (CAPAs).

  • Mentor and onboard junior colleagues, contributing to team knowledge sharing and development.

  • Travel to clinical sites as per monitoring plan (up to 60–75% travel required).

Qualifications & Experience:

  • Postgraduate degree in Life Sciences or related field.

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

  • Strong understanding of ICH-GCP guidelines and regulatory requirements.

  • Experience in FSP models is preferred but not mandatory.

  • Valid driver’s license where applicable.

Skills & Competencies:

  • Strong client management, communication, and interpersonal skills.

  • Knowledge of clinical research processes, medical terminology, and regulatory compliance.

  • Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC).

  • Excellent attention to detail, organizational skills, and ability to prioritize multiple projects.

  • Problem-solving skills, flexibility, and ability to work independently or in a team.

  • Familiarity with Risk-Based Quality Management (RBQM) monitoring concepts.

  • Digital literacy and proficiency in Microsoft Office.

  • Good English language and grammar skills.

Why Join Us:

  • Be part of a globally recognized CRO with opportunities to work across diverse therapeutic areas and trial models.

  • Exposure to both remote and on-site clinical trial monitoring, enhancing your career growth.

  • Collaborate with top pharmaceutical and biotech companies, contributing to life-changing therapies.

  • Supportive work environment with opportunities for mentoring, training, and professional development.

Apply Now: Contribute to advancing clinical research and ensure high-quality, compliant trials that impact patients’ lives globally.