MSc Chemistry Job at Sun Pharma | Apply Now for Clinical Research Associate Job
Are you looking for an MSc Chemistry job or a Clinical Research Associate job in Hyderabad with one of the leading pharmaceutical companies? Sun Pharma Laboratories Ltd is offering exciting jobs at Sun Pharma for professionals who want to build strong chemical science careers in clinical research. This opportunity is ideal for candidates with a background in chemistry, pharmacy, or life sciences who want to contribute to Phase III and Phase IV clinical trials while gaining experience in site management, regulatory compliance, and clinical study operations.
About Sun Pharma
At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an Sun Pharma Laboratories Ltd is a leading global pharmaceutical company headquartered in Mumbai, known for developing high-quality and affordable medicines across many therapeutic areas. The company operates in more than 100 countries and focuses strongly on research, innovation, and patient-centric healthcare solutions. Sun Pharma provides excellent opportunities for professionals seeking MSc chemistry jobs, clinical research associate jobs, and long-term chemical science careers in the pharmaceutical industry. With advanced research facilities and strong clinical development programs, the organization continues to create rewarding jobs
at Sun Pharma for talented candidates who want to grow, collaborate, and contribute to global healthcare advancements.- Job Title: Clinical Research Associate (Clinical Trials)
- Location: Hyderabad
Key Responsibilities:
- Perform site feasibility, identify potential investigators, negotiate study budget with potential investigators, finalize the investigators, sites, and execution of CDA and study-related contracts
- Preparation and submission of study documents for EC permission for the respective study across centers
- Oversee & document IP dispensing, inventory management & reconciliation
- Ensure timely site initiation, site monitoring, and site close-out activities are performed, and respective reports are generated
- Investigator and site personnel training on the Study protocol, procedures, and GCP principles
- Ensure timely recruitment of trial participants and subsequent efficient and effective data entry, source data verification, and query resolution
- Ensure timely reporting of SAEs, SUSARs, and reporting of SAEs to all sites and investigators in alignment with regulations and Suns PV policies
- Risk identification, analysis, and CAPA for sites not meeting expectations as per the plan
- Coordinate with in-house or CRO partners for data management, statistical analysis, statistical analysis report & DBL
Job Requirements
- Educational Qualification: Bachelor’s or Master’s degree in a health or related field, such as Biology, Chemistry, Nursing, Pharmacy, or Public Health, and/or Post-graduate Diploma in Clinical Research
- Experience: Relevant experience of 1-5 years minimum in the field of Clinical Research.
Additional Skills:
- Knowledge of GCP practices and regulatory guidelines in Clinical Trials
- Phase III and Phase IV Clinical Trials knowledge expertise
- Site Management expertise
- Collaboration with cross-functional stakeholders
