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Clinical Document Specialist

Novotech
NovoTech
2-5 years
Not Disclosed
India
10 April 6, 2026
Job Description
Job Type: Full Time 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 Document Specialist | Full-Time | India
Experience Required: 2-5 years

Job Description:
We are seeking a meticulous Clinical Document Specialist (CDS) to support clinical teams in India by managing and maintaining high-quality Trial Master Files (TMF) and essential clinical trial documents. This role ensures that all documentation processes align with regulatory requirements, project standards, and SOPs, facilitating smooth clinical operations and compliance.

Key Responsibilities:

  • Oversee the setup, maintenance, and quality control of Trial Master Files (TMF) for assigned projects.

  • Manage both electronic and paper TMF documents in accordance with project requirements, ICH-GCP guidelines, local/global regulatory standards, and company/client SOPs.

  • Ensure routine document management activities are completed accurately and on time.

  • Collaborate with internal and external clinical teams to track, file, and reconcile essential documents.

  • Support audits and inspections by providing organized and compliant documentation.

  • Implement and maintain document management best practices to enhance TMF efficiency and quality.

Qualifications & Experience:

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

  • 2-5 years of experience in clinical document management, TMF, or related clinical operations.

  • Strong knowledge of ICH-GCP, TMF management, and regulatory documentation standards.

  • Excellent organizational, analytical, and communication skills.

  • Ability to manage multiple priorities and ensure attention to detail under strict timelines.

Location: India (flexible across major cities)

Why Join Us:

  • Work on global clinical research projects with a focus on quality and compliance.

  • Gain hands-on experience in TMF management and clinical documentation best practices.

  • Opportunities for career development, professional growth, and cross-functional collaboration.