JSS Medical Research is a leading clinical research organization (CRO) known for its excellence in clinical trials and research studies. With a strong reputation in the industry, JSS Medical Research has received 3.2/5 ratings based on 102 reviews, reflecting its commitment to quality and innovation in clinical research.
Key Responsibilities
As a Clinical Research Associate (CRA), you will play a crucial role in ensuring the smooth execution of clinical trials. Your responsibilities will include:
✔ Site Selection & Qualification – Identify and assess potential study sites.
✔ Regulatory Compliance – Ensure submissions to Ethics Committees (EC) and approvals.
✔ Monitoring & Training – Conduct onsite & remote monitoring visits, verify source documents, CRFs, and train site staff.
✔ Patient Recruitment – Track enrollment and ensure study timelines are met.
✔ Audit Preparation – Prepare sites for internal/client audits & inspections.
✔ Documentation & Archival – Maintain study documents, including CRFs, CTM accountability, and source documents.
✔ Travel Requirement – 50-70% travel to various clinical sites.
Skills & Qualifications
✔ Education: Postgraduate in Life Sciences/Science/BDS/MDS/BAMS/BHMS.
✔ Experience: Minimum 2 years as a CRA with onsite monitoring experience.
✔ Technical Skills: Proficiency in MS Office, GCP (Good Clinical Practices), and GDP (Good Documentation Practices).
✔ Soft Skills: Strong communication, problem-solving, and multitasking abilities.
Why Join JSS Medical Research?
✅ Reputed Clinical Research Organization (CRO) with a strong industry presence.
✅ Opportunity to work on diverse clinical trials.
✅ Career growth in research & development.
✅ Competitive salary & benefits.
