Clinical Research Associate Jobs in Raptim Research Pvt. Ltd - Navi Mumbai, Maharashtra
Raptim Research Pvt. Ltd.
Navi Mumbai, Maharashtra, India
Posted on 19-01-2026
1 Vacancy
Description
- Job Title: Clinical Research Associate
- Qualification: BParm/MPharm
- Location: Raptim Research Pvt. Ltd- Navi Mumbai, Maharashtra
- Work Experience: 0 to 2 Years
Job Description
- Monitor clinical trial sites to ensure compliance with study protocol, GCP and regulatory requirements.
- Conduct site initiation, monitoring and close-out visits as per study plan.
- Verify source documents and case report forms for accuracy and completeness.
- Ensure proper informed consent process and patient safety throughout the trial.
- Review and report adverse events and serious adverse events in a timely manner.
- Check investigational product storage, accountability and reconciliation.
- Maintain trial master file and essential study documentation.
- Coordinate with investigators, study coordinators and sponsors for smooth trial conduct.
- Identify protocol deviations and support corrective and preventive actions.
- Prepare monitoring visit reports and follow up on outstanding issues.
Take this opportunity to join Raptim Research Pvt. Ltd - Navi Mumbai, Maharashtrar as a Clinical Research Associate in Navi Mumbai, Maharashtra and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.
Category
Clinical Research/ Data Science
Preferred Education
Key Skills
About Organization
Raptim Research Pvt. Ltd. is a global independent Clinical Research Organization (CRO) headquartered in Navi Mumbai, Maharashtra, providing end-to-end clinical development, bioequivalence, bioanalytical, and trial management services for pharmaceutical and biotech companies worldwide. It operates state-of-the-art clinical research facilities in Mumbai and Gandhinagar with regulatory-compliant infrastructure supporting Phase I–IV trials across multiple therapeutic areas. The company’s core focus is on delivering high-quality, globally regulated clinical research services, accelerating drug development with strong quality and compliance standards. The Clinical Research Associate (CRA) role typically involves monitoring clinical trial sites, ensuring adherence to protocols and Good Clinical Practice (GCP), and supporting documentation and regulatory compliance.
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