Raptim Research Hiring Clinical Research Associate (CRA)

Clinical Research Associate Jobs for B Pharm/M.Pharm/MSc in Navi Mumbai – 4+ Years Experience Required

Apply for Clinical Research Associate (CRA) vacancies in Navi Mumbai. Requires B Pharm, M.Pharm, or MSc with 4–5 years of monitoring experience in Respiratory & Ophthalmology clinical trials

Exciting Career Opportunity for Experienced Clinical Research Professionals

If you’re a clinical research professional seeking to advance your career in therapeutic domains like Respiratory and Ophthalmology, this is the perfect opportunity. Raptim Research is hiring Clinical Research Associates (CRAs) with 4–5 years of monitoring experience to join their growing team in Navi Mumbai. The role demands expertise in Good Clinical Practice (GCP), independent monitoring, and protocol compliance — essential for ensuring the success of regulated clinical trials.

About the Role

Clinical Research Associate (CRA) – Respiratory & Ophthalmology Trials

This CRA role is ideal for candidates who have prior hands-on monitoring experience, especially in therapeutic areas such as Respiratory and Ophthalmology. You’ll work closely with investigators and study sites to ensure protocol compliance, accurate data capture, and regulatory adherence.

Key Responsibilities:

• Conduct on-site and remote monitoring per the study-specific monitoring plan
• Ensure site adherence to ICH-GCP, regulatory requirements, and company SOPs
• Perform source document verification (SDV), CRF reviews, and query resolution
• Support site selection, initiation, monitoring, and close-out visits
• Collect and verify regulatory documents and ensure data integrity
• Maintain essential study documentation and timely reporting
• Collaborate with Project Managers, CTAs, and Data Management teams
• Proactively identify and escalate site performance issues

Who Should Apply?

This opportunity is best suited for candidates with:

• Minimum 4–5 years of clinical monitoring experience
• Educational background in B Pharm, M.Pharm, or MSc (Life Sciences)
• Strong understanding of GCP, regulatory compliance, and ethical trial conduct
• Excellent communication and documentation skills

Why Join Raptim Research?

Raptim Research is a recognized name in the Indian CRO industry. The company offers:

• Exposure to international-level clinical research standards
• Work on diverse therapeutic areas with highly regulated protocols
• Career growth for professionals with strong monitoring and trial oversight skills

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