Clinical Research Associate Job at Sun Pharma | Biology | Apply Now
Sun Pharmaceutical Industries Ltd., the fourth-largest specialty generic pharmaceutical company in the world, is inviting applications for the position of Clinical Research Associate (CRA) for its Hyderabad operations. This Clinical Research Associate Job is a pivotal role within the Clinical Research Business Unit, focused on managing the lifecycle of Phase III and Phase IV clinical trials. If you are looking to advance a Sun Pharma Career in a high-growth, “self-drive” environment that values continuous progress and collaboration, this position offers the ideal platform to manage multicenter trials and ensure the highest standards of Good Clinical Practice (GCP).
- Job Position: Clinical Research Associate (Clinical Trials)
- Location: Hyderabad
- Business Unit: Clinical Research
About the Company
Sun Pharma focuses on fostering an environment where employees are encouraged to “Take charge” and become “Better every day”. A Sun Pharma Career is defined by a “Thrive together” spirit, emphasizing support for each other’s professional journeys. Joining the fourth-largest generic pharma company means participating in large-scale studies that have a lasting impact on global healthcare. The company provides robust benefits and a culture aimed at prioritizing employee success and well-being.
Job Overview
In this Clinical Research Job, the CRA acts as the primary link between the sponsor (Sun Pharma) and the study sites (hospitals/clinics).
- Site Identification & Feasibility: Perform feasibility assessments to identify potential investigators and negotiate study budgets.
- Regulatory Compliance: Prepare and submit essential study documents for Ethics Committee (EC) permissions across multiple centers.
- Training & GCP Adherence: Conduct investigator and site personnel training on study protocols, procedures, and Good Clinical Practice (GCP) principles.
- Monitoring Lifecycle: Ensure timely site initiation, routine monitoring visits, and close-out activities, including the generation of detailed monitoring reports.
- IP & Logistics: Oversee investigational product (IP) dispensing, inventory management, and reconciliation to ensure accountability.
- Data Integrity: Facilitate trial participant recruitment and ensure effective data entry, source data verification (SDV), and query resolution.
Key Responsibilities
The CRA is responsible for maintaining the safety profile and data quality of the ongoing trial.
- Safety Reporting: Ensure timely reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs) in alignment with regulations and Sun’s Pharmacovigilance (PV) policies.
- Risk Management: Identify and analyze risks at sites not meeting expectations and implement Corrective and Preventive Actions (CAPA).
- Data Management Coordination: Partner with in-house or CRO (Contract Research Organization) teams for data management, statistical analysis, and Database Lock (DBL).
- Stakeholder Collaboration: Maintain close collaboration with cross-functional stakeholders to ensure study milestones are met on time.
Requirements for the Clinical Research Job
Sun Pharma is seeking candidates with a strong foundation in health sciences and practical field experience.
- Education: Bachelor’s or Master’s degree in Biology.
- Advanced Training: A Post-graduate Diploma in Clinical Research is highly desirable.
- Experience: A minimum of 1–5 years of relevant experience in the field of Clinical Research.
- Specialized Knowledge: Proven expertise in Phase III and Phase IV clinical trials and site management.
- Regulatory Grasp: In-depth knowledge of GCP practices and global regulatory guidelines governing clinical trials.
- Soft Skills: Strong interpersonal skills for negotiating contracts (CDA) and study budgets with investigators.
In summary, this Clinical Research Associate Job at Sun Pharma Hyderabad is a definitive career move for those ready to lead “on the ground” trial operations. A Sun Pharma Career offers the unique opportunity to manage the complexities of late-phase clinical trials within a world-class pharmaceutical framework. Because the role demands high-level site management and strict regulatory adherence, your ability to conduct source data verification and manage SAE reporting will be your greatest assets. If you have the drive to “Create your own sunshine” in the biotech sector, this role is your platform to excel.
