Exciting Clinical Research Associate Job at Sun Pharma Hyderabad offering site management, monitoring responsibilities, and career growth in clinical research.
Sun Pharma Laboratories Ltd, one of India’s leading and globally recognized pharmaceutical organizations, invites applications for the role of Clinical Research Associate (Clinical Trials). Based at the Sun House Corporate Office in Hyderabad, this position offers a meaningful opportunity for professionals passionate about clinical operations, regulatory compliance, and contributing to high-quality clinical research outcomes. Clinical Research Associate Job at Sun Pharma
Sun Pharma is known for creating an environment that motivates individuals to grow, learn, innovate, and take ownership of their career journey. Through its culture of collaboration, continuous development, and empowerment, Sun Pharma inspires employees to become “better every day.” This role is ideal for candidates who aspire to make a lasting impact in the clinical trial landscape while working with one of the most respected pharmaceutical brands in India. Clinical Research Associate Job at Sun Pharma
About Sun Pharma’s Clinical Research Environment
Stepping into the Sun Pharma ecosystem means joining an organization that strongly believes in professional excellence, transparent processes, and scientific advancement. The Clinical Research division works across phases of drug development, ensuring that studies follow regulatory guidelines, maintain ethical integrity, and deliver reliable results. As a Clinical Research Associate, you will play a pivotal role in study execution, site performance, training, and safeguarding participant safety. Clinical Research Associate Job at Sun Pharma
The company emphasizes three foundational principles:
- Take Charge – Demonstrate ownership, initiative, and confidence while managing clinical responsibilities.
- Better Every Day – Achieve continuous improvement through learning, skill enhancement, and process optimization.
- Thrive Together – Collaborate with colleagues, investigators, and cross-functional teams to ensure successful study delivery.
With these guiding values, Sun Pharma fosters a workplace where every team member is supported and empowered to achieve excellence. Clinical Research Associate Job at Sun Pharma
Key Highlights of the Position
Job Title: Clinical Research Associate
Business Unit: Clinical Research
Location: Hyderabad (Sun House Corporate Office)
Experience Required: 1–5 years in Clinical Research
Qualification: Bachelor’s or Master’s in Life Sciences or related fields
Trial Phases: Experience in Phase III and Phase IV preferred
Key Responsibilities
As a Clinical Research Associate at Sun Pharma, your role encompasses the comprehensive management and oversight of clinical trial sites. Your responsibilities will span feasibility assessment, site initiation, monitoring, reporting, training, compliance, and ensuring that study outcomes are achieved in alignment with regulatory standards. Clinical Research Associate Job at Sun Pharma
1. Site Feasibility and Investigator Selection
You will be responsible for evaluating potential study sites based on capabilities, infrastructure, patient pool, and readiness to conduct the proposed clinical trial. This includes:
- Identifying qualified investigators.
- Conducting feasibility assessments.
- Discussing and negotiating study budgets with investigators.
- Finalizing investigators and sites.
- Overseeing the execution of clinical trial agreements (CTAs), confidentiality agreements (CDAs), and other contractual documents.
This process ensures that each study site can effectively meet the operational requirements of the clinical trial. Clinical Research Associate Job at Sun Pharma
2. Documentation and Ethics Committee Submission
The CRA plays a key role in ensuring that all necessary study documentation is prepared and submitted to the Institutional Ethics Committees (IECs) across participating centers. Responsibilities include:
- Preparing study-specific documents according to protocol needs.
- Ensuring timely submission for ethics review and approval.
- Maintaining regulatory binders and ensuring compliance with applicable guidelines.
Strong attention to detail is crucial to maintaining thorough and accurate documentation throughout the study lifecycle.
3. Investigational Product (IP) Management
Proper management of the Investigational Product is essential in any clinical study. The CRA will: Clinical Research Associate Job at Sun Pharma
- Oversee IP dispensing processes at study sites.
- Monitor inventory, storage conditions, and protocol compliance.
- Document reconciliation and ensure accurate records throughout the study.
This ensures accountability and prevents discrepancies that may impact study quality.
4. Site Initiation, Monitoring, and Close-Out
The CRA ensures operational excellence at every stage of site management, including:
- Conducting structured site initiation visits.
- Ensuring training on the protocol, GCP, and study-specific procedures.
- Performing routine monitoring visits to verify data accuracy, consent process adherence, and protocol compliance.
- Generating detailed monitoring reports.
- Ensuring corrective actions where needed.
- Completing site close-out activities and verifying all study materials are returned or archived.
Monitoring ensures that data integrity, participant safety, and regulatory compliance are consistently maintained. Clinical Research Associate Job at Sun Pharma
5. Training of Investigators and Site Personnel
Training is a key part of maintaining quality across all study centers. You will:
- Train investigators and study coordinators on protocol requirements.
- Provide guidance on Good Clinical Practices (GCP).
- Clarify study procedures and operational expectations.
- Reinforce compliance through routine communication and support.
Effective training directly contributes to improved site performance and reduced protocol deviations. Clinical Research Associate Job at Sun Pharma
6. Ensuring Timely Recruitment and Data Quality
A major responsibility includes oversight of patient recruitment and data management. Key tasks include:
- Ensuring timely enrollment of trial participants.
- Monitoring data entry for completeness and accuracy.
- Conducting source data verification (SDV).
- Coordinating query resolution with the site and data management team.
This ensures that the study timelines are met and that the collected data meets the highest standards of reliability.
7. Safety Reporting and Regulatory Compliance
Patient safety is the highest priority in clinical trials. The CRA is responsible for:
- Ensuring timely reporting of Serious Adverse Events (SAEs).
- Ensuring SUSAR reporting in accordance with regulatory timelines.
- Communicating safety updates to investigators across sites.
- Maintaining compliance with pharmacovigilance (PV) policies and regulatory guidelines.
Proper safety reporting helps identify risks early and protects study participants’ well-being. Clinical Research Associate Job at Sun Pharma
8. Risk Identification and CAPA Implementation
You will monitor site performance and identify any risks or deviations from the study plan. Responsibilities include:
- Analyzing site performance metrics.
- Identifying potential risks in recruitment, protocol adherence, or data quality.
- Implementing Corrective and Preventive Actions (CAPA).
- Ensuring ongoing improvement and immediate resolution of study challenges.
This proactive approach ensures smooth study execution and regulatory readiness.
9. Coordination with Internal and External Stakeholders
As the bridge between Sun Pharma, investigators, CRO partners, and data management teams, you will:
- Collaborate with CROs for data management, biostatistics, and database lock (DBL).
- Support coordination for statistical analysis reports.
- Maintain effective communication among all functional teams.
- Ensure that each stage of study execution aligns with overall project timelines.
Collaboration ensures accuracy, efficiency, and successful study completion.
Job Requirements
Educational Qualification
Candidates should possess: Clinical Research Associate Job at Sun Pharma
- A Bachelor’s or Master’s degree in a related discipline such as Biology, Chemistry, Nursing, Pharmacy, Public Health, or Life Sciences.
- A Post-Graduate Diploma in Clinical Research will be considered an added advantage.
Experience
- Minimum 1 to 5 years of experience in clinical research.
- Hands-on experience in managing Phase III and Phase IV trials is highly desirable.
Additional Skills
- Strong knowledge of GCP principles and clinical trial regulations.
- Excellent site management and communication skills.
- Ability to collaborate with cross-functional teams.
- Strong analytical and documentation skills.
- Problem-solving capabilities essential for addressing site-level challenges.
Key Highlights
Position: Clinical Research Associate
Department: Clinical Research
Location: Hyderabad
Experience: 1–5 years
Trial Phase Expertise: Phase III and Phase IV
Core Skills: GCP knowledge, site monitoring, documentation, IP handling, safety reporting, stakeholder coordination
Why Join Sun Pharma?
Sun Pharma places significant emphasis on professional growth and employee well-being. The company ensures: Clinical Research Associate Job at Sun Pharma
- A dynamic learning environment
- Collaborative working culture
- Opportunities to work across diverse clinical programs
- Exposure to global-standard research processes
- Robust support for personal and professional development
Sun Pharma strongly values employees who demonstrate initiative, curiosity, and commitment to excellence. Clinical Research Associate Job at Sun Pharma
How to Apply
Interested and eligible candidates can apply by visiting the official Sun Pharma careers page. Candidates should prepare an updated resume, highlight relevant clinical research experience, and ensure that all documents are ready for submission.
For direct application, follow the steps: Clinical Research Associate Job at Sun Pharma
- Visit the official Sun Pharma Careers Portal.
- Search for the position titled Clinical Research Associate – Clinical Trials.
- Complete the online application form and upload your resume.
- Submit the application and monitor your email for updates from the recruitment team.
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Note: This job information is sourced from publicly available official sources. We share it for reference purposes only and do not claim ownership of the job posting.
