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Clinical Trial Associate

Sun Pharma
Sun Pharma
0-2 years
Not Disclosed
Mumbai, India
10 April 14, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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 Trial Associate – Mumbai | Clinical Research | Pharma Jobs

Company: Sun Pharma Laboratories Ltd
Location: Mumbai
Job Type: Full-Time
Work Mode: On-site
Experience: 0–2 Years
Qualification: Life Sciences / Pharmacy / Nursing / Public Health / Clinical Research


Job Overview

Start your career in clinical research with a role that puts you at the center of clinical trial operations. As a Clinical Trial Associate (CTA), you will support documentation, regulatory compliance, and site coordination activities across ongoing clinical studies.

This position is ideal for freshers or early-career professionals aiming to build expertise in clinical trials, regulatory submissions, and GCP-compliant research environments within a leading pharmaceutical company.


Key Responsibilities

Documentation & Trial Support

  • Assist in maintaining study documents such as protocols, informed consent forms (ICF), case report forms (CRFs), and study reports
  • Organize and manage Trial Master File (TMF) documentation (electronic and paper-based)
  • Ensure accuracy, completeness, and audit readiness of study files

Regulatory Compliance Support

  • Support preparation and submission of regulatory documents to Ethics Committees (EC) and health authorities
  • Ensure adherence to ICH-GCP guidelines, SOPs, and local regulatory requirements
  • Assist in maintaining compliance documentation for audits and inspections

Site Coordination & Operations

  • Track site invoices and support payment processing
  • Manage vendor code generation and vendor tracking activities
  • Coordinate with internal teams and study sites for smooth study execution

Administrative & Communication Support

  • Schedule meetings, prepare meeting minutes, and maintain communication logs
  • Support travel coordination and logistics for study-related activities
  • Assist cross-functional teams in day-to-day clinical operations

Required Skills & Qualifications

Educational Requirements

  • Bachelor’s or Master’s degree in:
    • Life Sciences
    • Pharmacy
    • Nursing
    • Public Health
  • OR Postgraduate Diploma in Clinical Research

Experience

  • 0–2 years of experience in Clinical Research / CTA role

Core Skills & Technical Knowledge

  • Basic understanding of clinical trial processes and documentation
  • Knowledge of ICH-GCP guidelines and regulatory requirements
  • Familiarity with CRFs, TMF, and clinical study documentation
  • Exposure to regulatory submissions and compliance processes (preferred)

Soft Skills

  • Strong organizational and documentation skills
  • Good communication and coordination abilities
  • Attention to detail and ability to manage multiple tasks
  • Ability to work in a team-oriented clinical research environment

Perks & Benefits

  • Entry into the clinical research and pharmaceutical industry
  • Hands-on exposure to clinical trial operations and regulatory processes
  • Learning and development opportunities in GCP and clinical data handling
  • Career growth into CRA, Clinical Operations, or Regulatory roles
  • Collaborative and structured work environment

About the Company

Sun Pharma Laboratories Ltd is a global pharmaceutical leader known for its innovation in generics and specialty medicines. With strong capabilities in clinical research and regulatory excellence, the company is committed to advancing healthcare and improving patient outcomes worldwide.


Salary / Compensation

💰 Not disclosed (Competitive entry-level package)


Work Mode

📍 On-site – Mumbai, India


Call to Action

If you’re looking to start your career in clinical trials and regulatory research, this role offers the perfect foundation.

👉 Apply now and begin your journey in clinical research with a leading pharmaceutical company.