Sun Pharma Hiring Clinical Research Associate (Clinical Trials) – Hyderabad
- Pharma Clinical Research Jobs Sun Pharma
- Company Overview
- Job Role and Responsibilities
- Eligibility and Qualifications
- Required Education
- Experience
- Required Skills
- Location and Salary
- Application Process
- Frequently Asked Questions
- What does a Clinical Research Associate do?
- What qualifications are required for this role?
- How much experience is required for this position?
- What clinical trial phases will I work on?
- How can I apply for this job?
- Job Summary
Pharma Clinical Research Jobs Sun Pharma
Sun Pharma Laboratories Ltd is currently hiring for the position of Clinical Research Associate (CRA) in the Clinical Research department. The opportunity is based in Hyderabad at the Sun House Corporate Office. This role is suitable for professionals with 1–5 years of experience in clinical trials and pharmaceutical research who want to work on regulated drug development studies and contribute to advancing patient care through evidence‑based clinical research.
The position offers a chance to work closely with investigators, research sites, ethics committees, and cross‑functional clinical operations teams. Professionals joining this role will be involved in monitoring clinical trial activities, ensuring regulatory compliance, and supporting the execution of Phase III and Phase IV clinical studies. For candidates seeking long‑term careers in pharmaceutical clinical research, this opportunity provides valuable exposure to industry‑standard clinical trial operations and global regulatory practices.
Company Overview
Sun Pharma Laboratories Ltd is one of the largest pharmaceutical companies in India and a globally recognized manufacturer of specialty and generic medicines. The company operates across more than 100 countries and focuses on delivering high‑quality, affordable medicines that improve patient outcomes worldwide.
Sun Pharma invests significantly in pharmaceutical research, clinical trials, regulatory science, and innovative drug development. Its clinical research division plays a vital role in evaluating the safety and effectiveness of medicines through carefully designed clinical trials conducted according to international regulatory standards.
The company fosters a professional work culture that encourages continuous learning, collaboration, and innovation. Employees are supported with growth opportunities that allow them to develop expertise in clinical operations, regulatory affairs, drug safety, and pharmaceutical research.
Through its commitment to scientific excellence and ethical research practices, Sun Pharma continues to contribute to the advancement of global healthcare and the development of life‑saving therapies.
Job Role and Responsibilities
The Clinical Research Associate will support the planning, coordination, and monitoring of clinical trials conducted by Sun Pharma. The role requires strong knowledge of clinical research processes, Good Clinical Practice (GCP) guidelines, and regulatory compliance standards.
Key responsibilities include:
- Conduct site feasibility assessments and identify potential investigators for clinical studies
- Negotiate study budgets with investigators and finalize study sites
- Execute confidentiality disclosure agreements (CDA) and clinical trial contracts
- Prepare and submit regulatory documentation to Ethics Committees for study approvals
- Monitor investigational product (IP) dispensing, inventory tracking, and reconciliation activities
- Ensure timely site initiation visits, monitoring visits, and site close‑out procedures
- Train investigators and site staff on clinical study protocols and GCP principles
- Ensure timely recruitment of study participants and maintain accurate trial documentation
- Perform source data verification and support clinical data management activities
- Ensure prompt reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs)
- Support regulatory reporting requirements in alignment with Sun Pharma pharmacovigilance policies
- Identify operational risks at research sites and implement corrective and preventive actions (CAPA)
- Collaborate with internal clinical teams, data management specialists, statisticians, and CRO partners
This role plays an important part in ensuring clinical trials are conducted ethically, safely, and in compliance with international regulatory standards.
Eligibility and Qualifications
Candidates interested in this pharmaceutical clinical research role must meet the following educational and professional requirements.
Required Education
Bachelor’s or Master’s degree in a healthcare or life sciences discipline.
Relevant courses include:
Pharmacy, Clinical Research, Biotechnology, Biochemistry, Microbiology, Life Sciences, Biomedical Sciences, Nursing, Public Health, Pharmacology, Molecular Biology, Chemistry
A Post‑Graduate Diploma in Clinical Research is also considered relevant for this position.
Experience
- Minimum 1–5 years of experience in clinical research or clinical trial operations
- Experience working with pharmaceutical companies, contract research organizations, or hospital research sites is preferred
Required Skills
- Strong understanding of Good Clinical Practice (GCP) guidelines
- Knowledge of regulatory requirements governing clinical trials
- Experience in Phase III and Phase IV clinical trials
- Site management and monitoring expertise
- Strong documentation and clinical data verification skills
- Ability to collaborate with cross‑functional teams and external research partners
Professionals with experience in clinical monitoring, investigator coordination, and trial documentation will find this role highly aligned with their expertise.
Location and Salary
Job Location: Hyderabad, India
Application Process
Candidates who meet the eligibility criteria can apply directly through the official Sun Pharma careers portal.
Apply here:
https://careers.sunpharma.com/job/Mumbai-Clinical-Research-Associate-%28Clinical-Trials%29/48646544/
Applicants are advised to apply only through the official company website to ensure authenticity and avoid recruitment scams.
Frequently Asked Questions
What does a Clinical Research Associate do?
A Clinical Research Associate monitors clinical trials to ensure that research studies follow regulatory guidelines, ethical standards, and approved study protocols. The role involves site monitoring, data verification, and coordination with investigators and clinical teams.
What qualifications are required for this role?
Candidates should have a bachelor’s or master’s degree in life sciences such as Pharmacy, Biotechnology, Biochemistry, Nursing, or Public Health. A diploma in clinical research can also support eligibility.
How much experience is required for this position?
The company requires candidates with approximately 1–5 years of experience in clinical research or pharmaceutical trial monitoring.
What clinical trial phases will I work on?
This role involves supporting Phase III and Phase IV clinical trials related to pharmaceutical drug development.
How can I apply for this job?
Candidates can apply through the official Sun Pharma careers website using the application link provided in this article.
Job Summary
| Company | Sun Pharma Laboratories Ltd |
|---|---|
| Vacancies | Clinical Research Associate (Clinical Trials) |
| Required Education | Pharmacy, Clinical Research, Biotechnology, Biochemistry, Microbiology, Life Sciences, Biomedical Sciences, Nursing, Public Health, Pharmacology, Molecular Biology, Chemistry |
| Experience | 1–5 years Clinical Research experience |
To apply for this job please visit careers.sunpharma.com.
