Curaclin SMO is hiring qualified candidates with a background in Pharmacy, Life Sciences, or Clinical Research. This opportunity is ideal for professionals seeking growth in clinical trials, site management, and GCP-compliant research environments.
If you have experience in clinical research coordination, patient recruitment, and regulatory documentation, this role offers excellent exposure to real-world clinical trials.
🔬 Job Overview
- Position: Clinical Research Coordinator
- Company: Curaclin SMO
- Location: Bhubaneswar, Odisha
- Employment Type: Full-time
- Industry: Clinical Research / Pharma / Life Sciences
📋 Key Responsibilities
As a Clinical Research Coordinator, you will:
- Coordinate and manage clinical trial activities at the site
- Assist the Principal Investigator (PI) in study conduct as per protocol
- Handle patient screening, recruitment, and follow-ups
- Maintain study documentation and regulatory files
- Ensure compliance with ICH-GCP guidelines and protocol requirements
- Perform data entry and query resolution
- Coordinate with sponsors, CROs, and site staff
- Support monitoring visits, audits, and inspections
🎓 Qualifications Required
Candidates applying for this clinical research job in India should have:
- B.Pharm / M.Pharm / Life Sciences / Pharmacy degree
- Strong understanding of Clinical Research & GCP guidelines
- Good communication and documentation skills
- Prior experience in site management or clinical trials (preferred)
💼 Benefits & Career Growth
- Hands-on experience in clinical trial management
- Opportunity to work with leading sponsors and CROs
- Exposure to regulatory compliance and audits
- Career advancement in the clinical research industry
- Professional development in ICH-GCP practices
📩 How to Apply
Interested candidates can apply by sending their updated resume to:
📧 Email: hr@curaclinsmo.com
