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If you’re an experienced Clinical Research Associate (CRA) looking to advance your career in clinical operations, this is an excellent opportunity. As clinical research in India continues to expand, our partner Clinovo is hiring skilled CRA professionals across major Indian cities. This role is ideal for candidates with strong on-site monitoring experience and a passion for high-quality clinical trial execution.
📍 Job Locations
Openings available in the following cities:
Mumbai, Bengaluru, Chennai, Delhi, Kolkata, Pune
🔹 Key Responsibilities
As a Clinical Research Associate, your responsibilities will include:
- Conducting site selection, initiation, monitoring, and close-out visits per ICH-GCP guidelines
- Supporting and tracking subject recruitment at the site level
- Providing protocol training and maintaining effective site communication
- Ensuring regulatory compliance, data quality, and timely CRF completion
- Managing study progress — submissions, approvals, enrollment & query resolution
- Maintaining essential documents in the Trial Master File (TMF) and reviewing ISFs
- Preparing clear monitoring reports, follow-up letters, and documentation
- Collaborating with cross-functional study teams
✔ Required Qualifications
Candidates must have:
- Bachelor’s degree in life sciences/healthcare
- 2–3 years of on-site monitoring experience (mandatory)
- Strong understanding of ICH-GCP and clinical protocols
- Good therapeutic area knowledge
- Proficiency in MS Word, Excel, PowerPoint
- Excellent communication, organization, and problem-solving skills
- Ability to build strong site and team relationships
✨ Benefits of Joining
- Exposure to global-standard clinical research operations
- Opportunity to work on impactful and innovative clinical trials
- Career advancement in a rapidly expanding clinical research environment
- Collaborative and supportive cross-functional teams
📨 How to Apply
Eligible and interested candidates can send their latest resume to:
📧 akhila.kasipogu@clinovo.com