Company Description JSR Pharma Solutions is a growing pharmaceutical services organization focused on supporting the development and delivery of safe, effective therapies. The company collaborates with biopharma partners to advance clinical programs through high-quality operations, data integrity, and regulatory compliance.

JSR Pharma Solutions emphasizes a culture of accountability, continuous improvement, and cross-functional teamwork. Team members are encouraged to contribute ideas, build expertise, and support innovation in clinical research.

Role Description -Clinical Trial Associate a full-time hybrid role based in Hyderabad, with flexibility for partial work from home. This role supports clinical operations teams in planning, organizing, and executing clinical trials according to protocol, regulatory requirements, and company standards.

Day-to-day responsibilities include maintaining and updating the Trial Master File (TMF), tracking study documents, supporting informed consent processes, and assisting with site communications and coordination.

The Clinical Trial

Associate will help prepare regulatory and ethics submissions, schedule and document study meetings, and support monitoring activities and issue follow-up. The role also involves ongoing collaboration with cross-functional teams, accurate documentation, and adherence to timelines and quality expectations.





Qualifications

- PharmD/Bpharm/Mpharm/BSC/MSC/Btech
- 0-2 year experience in clinical research
- Freshers most welcome
- Candidates should possess skills in Clinical Trials and Clinical Operations, including understanding of study workflows and regulatory requirements.
- Candidates should possess skills in Trial Master File (TMF) management, including organization, tracking, and quality review of essential documents.
- Candidates should possess knowledge of Informed Consent processes, including documentation standards and participant communication support.
- Candidates should possess Research skills, including information gathering, data handling, and attention to detail in documentation.
- Strong written and verbal communication skills, with the ability to collaborate effectively with internal teams and study sites.
- Excellent organizational, time-management, and prioritization abilities, with a focus on accuracy and compliance.
- Proficiency with MS Office and clinical trial management or document management systems; familiarity with GCP and ICH guidelines is beneficial.
- Bachelor’s degree in life sciences, pharmacy, nursing, or a related field; prior experience in a clinical research or pharmaceutical setting is an advantage.
- [email protected]

📌 Clinical Trial Associate (Hyderabad)
🏢 JSR Pharma Solutions
📍 Hyderabad