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Clinical Research Associate

Sun Pharma
Sun Pharma
1-5 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 Research Associate – Mumbai | Clinical Trials | Pharma Jobs

Company: Sun Pharma Laboratories Ltd
Location: Mumbai
Job Type: Full-Time
Work Mode: On-site
Experience: 1–5 Years
Qualification: Life Sciences / Pharmacy / Nursing / Public Health / Clinical Research


Job Overview

Step into a high-impact role in clinical research where you directly contribute to the execution of clinical trials and drug development. As a Clinical Research Associate (CRA), you will be responsible for site management, monitoring activities, regulatory compliance, and ensuring data integrity across clinical studies.

This role is ideal for professionals looking to build a strong career in clinical trials, pharmacovigilance, and regulatory compliance within a leading pharmaceutical organization.


Key Responsibilities

Clinical Trial Operations & Monitoring

  • Conduct site feasibility assessments and identify potential investigators
  • Initiate, monitor, and close clinical trial sites as per study timelines
  • Ensure proper documentation and reporting of site activities

Regulatory & Compliance Management

  • Prepare and submit study documents for Ethics Committee (EC) approvals
  • Ensure compliance with ICH-GCP, regulatory guidelines, and SOPs
  • Monitor SAE/SUSAR reporting in alignment with pharmacovigilance policies

Data Management & Quality Assurance

  • Perform source data verification (SDV) and ensure accurate data entry
  • Resolve data queries and ensure timely database lock (DBL) readiness
  • Coordinate with CROs and internal teams for data management and statistical analysis

Investigational Product (IP) Management

  • Oversee IP dispensing, inventory management, and reconciliation
  • Maintain compliance with study protocols and documentation standards

Stakeholder Coordination

  • Train investigators and site staff on protocols and GCP principles
  • Collaborate with cross-functional teams (Data Management, Biostatistics, PV)
  • Manage study timelines, risks, and CAPA for underperforming sites

Required Skills & Qualifications

Educational Requirements

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

Experience

  • 1–5 years of experience in Clinical Research / CRA role

Core Skills & Technical Expertise

  • Strong knowledge of ICH-GCP, clinical trial processes, and regulatory compliance
  • Experience in site monitoring, SDV, and clinical data management
  • Understanding of SAE, SUSAR reporting and pharmacovigilance processes
  • Familiarity with EDC systems, CRFs, and clinical databases
  • Knowledge of CAPA, risk management, and audit readiness

Soft Skills

  • Strong communication and stakeholder management skills
  • High attention to detail and problem-solving ability
  • Ability to manage multiple sites and deadlines

Perks & Benefits

  • Opportunity to work with a leading global pharmaceutical company
  • Exposure to end-to-end clinical trial lifecycle
  • Career growth in clinical research and drug development
  • Learning and development programs in regulatory and clinical domains
  • Collaborative and performance-driven work environment

About the Company

Sun Pharma Laboratories Ltd is one of the largest pharmaceutical companies globally, specializing in generics and specialty medicines. With a strong focus on clinical research, regulatory excellence, and innovation, Sun Pharma plays a key role in advancing healthcare and improving patient outcomes worldwide.


Salary / Compensation

💰 Not disclosed (Competitive industry-standard package)


Work Mode

📍 On-site – Mumbai, India


Call to Action

If you’re looking to build a strong career in clinical trials, pharmacovigilance, and regulatory affairs, this is your opportunity.

👉 Apply now and take the next step in your clinical research career with a global pharma leader.