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Country Approval Specialist

Thermo Fisher Scientific
Thermo Fisher Scientific
3-5 years
Not Disclosed
10 Jan. 20, 2026
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

Country Approval Specialist – Clinical Trial Submissions

Company: [Insert Company Name]
Location: Mumbai, Mahārāshtra, India (Remote/Hybrid options may apply)
Job Type: Full-Time
Category: Clinical Research / Regulatory Affairs
Experience Required: 3 – 5 years in regulatory submissions or clinical trial approvals


Job Overview

We are looking for a Country Approval Specialist to join our global clinical research team. This role is responsible for preparing, submitting, and managing country-specific regulatory dossiers for clinical trial approvals in India. The Specialist will ensure timely regulatory submissions, maintain compliance with local and international regulations, and serve as a key liaison between investigators, regulatory authorities, and cross-functional project teams.

This position is ideal for candidates who are detail-oriented, regulatory-savvy, and experienced in DCGI and Ethics Committee (EC) submissions within clinical trials.


Key Responsibilities

Regulatory Submissions & Approvals

  • Prepare country-specific clinical trial submission dossiers for DCGI and Ethics Committee approvals

  • Implement submission strategies to obtain regulatory approvals efficiently

  • Forecast timelines for submission and approval processes, ensuring study startup milestones are met

  • Liaise with regulatory authorities and investigators to facilitate approvals

Cross-Functional Collaboration

  • Collaborate with clinical operations, data management, and project teams to ensure timely and accurate documentation

  • Obtain, review, and maintain essential regulatory and clinical trial documents

  • Update and maintain regulatory systems for ongoing trials

Compliance & Guidance

  • Ensure compliance with Indian GCP, DCGI regulations, and international clinical trial guidelines

  • Provide guidance and support to project teams on regulatory requirements, submission timelines, and strategy

  • Manage amendments, notifications, and ongoing regulatory submissions for active studies


Qualifications & Experience

Education:

  • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Clinical Research, or related field

Experience:

  • 3 – 5 years experience in regulatory submissions or clinical trial approvals

  • Strong working knowledge of DCGI, Ethics Committee, and local regulatory frameworks

  • Experience in clinical trial documentation, dossier preparation, and submission management

Skills & Competencies:

  • Excellent attention to detail and organizational skills

  • Strong written and verbal communication skills in English

  • Ability to work effectively in cross-functional teams

  • Proficiency in regulatory submission tools and document management systems

  • Knowledge of global clinical trial guidelines (ICH-GCP) and local regulations


Career Growth & Global Exposure

  • Work with international clinical teams and stakeholders on multiple therapeutic areas

  • Develop expertise in regulatory strategies, submission processes, and country-specific approvals

  • Opportunity to progress to Senior Regulatory Affairs Specialist / Regulatory Manager roles


Why Join Us

  • Global Exposure: Collaborate with international teams and regulatory authorities

  • Professional Growth: Structured learning, mentoring, and career development pathways

  • Impact: Play a key role in ensuring compliance and timely approvals for clinical trials in India

  • Innovation: Work with modern regulatory systems and tools supporting global study delivery