Clinical Research Associate (Clinical Trials)
Company: Sun Pharma Laboratories Ltd
Business Unit: Clinical Research
Location: Hyderabad, India
Job Type: Full-Time
Experience Required: 1–5 Years
Education: Bachelor’s or Master’s degree in Life Sciences / Health Sciences (Biology, Chemistry, Nursing, Pharmacy, Public Health) and/or Postgraduate Diploma in Clinical Research
Posted On: February 13, 2026
About the Company
Sun Pharma Laboratories Ltd is one of India’s leading pharmaceutical organizations, committed to advancing global healthcare through high-quality, affordable medicines and robust clinical research programs. The organization fosters a performance-driven and growth-oriented work environment, enabling professionals to build meaningful careers in clinical development and regulatory sciences.
Job Overview
The Clinical Research Associate (CRA) will be responsible for end-to-end site management activities in Phase III and Phase IV clinical trials. This role involves site feasibility assessment, regulatory submissions, monitoring visits, compliance oversight, pharmacovigilance reporting, and collaboration with cross-functional stakeholders and CRO partners.
This opportunity is ideal for professionals seeking growth in clinical trial monitoring, GCP compliance, and regulatory-driven research operations.
Key Responsibilities
Conduct site feasibility assessments and identify potential investigators
Negotiate study budgets and finalize investigators, sites, and confidentiality agreements (CDA)
Execute clinical trial agreements and ensure regulatory documentation readiness
Prepare and submit study documents to Ethics Committees (EC) across multiple centers
Oversee Investigational Product (IP) dispensing, inventory management, and reconciliation
Perform site initiation, monitoring, and close-out visits with accurate report generation
Train investigators and site staff on study protocol, procedures, and Good Clinical Practice (GCP) guidelines
Ensure timely subject recruitment and data quality through source data verification (SDV) and query resolution
Ensure timely reporting of SAEs and SUSARs in alignment with regulatory requirements and pharmacovigilance policies
Identify site-level risks, perform root cause analysis, and implement CAPA strategies
Coordinate with internal teams or CRO partners for data management, statistical analysis, and database lock (DBL) activities
Required Skills and Competencies
Strong knowledge of ICH-GCP guidelines and regulatory frameworks governing clinical trials
Hands-on experience in Phase III and Phase IV clinical trials
Site management and monitoring expertise
Excellent documentation and compliance skills
Strong communication and stakeholder collaboration abilities
Risk assessment and corrective action planning capabilities
Why Join Sun Pharma
At Sun Pharma Laboratories Ltd, employees benefit from structured learning opportunities, professional development pathways, and exposure to global clinical research standards. The organization emphasizes ethical research practices, regulatory compliance, and collaborative growth to drive innovation in patient-centric healthcare solutions.
Disclaimer
This job description outlines the general nature and responsibilities of the role. Duties and responsibilities may evolve based on organizational requirements and business needs. The employer reserves the right to modify or assign additional responsibilities in alignment with the candidate’s experience and qualifications.
SEO Keywords: Clinical Research Associate Jobs in Hyderabad, CRA Jobs in India, Clinical Trials Jobs 2026, Phase III Clinical Research Careers, GCP Clinical Monitoring Jobs, Pharmacovigilance Reporting Roles, Clinical Trial Site Management Careers.
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