Clinical Research Coordinator

🚀 WE’RE HIRING – CLINICAL RESEARCH COORDINATOR 🚀

Looking to grow your career in clinical research and healthcare operations? Health Care Global Enterprises (HCG Hospitals) is hiring Clinical Research Coordinators for its Vadodara location. This is an excellent opportunity for candidates with experience in clinical trial coordination, patient management, regulatory compliance, and study documentation who want to work in a professional clinical research environment with exposure to oncology and advanced healthcare studies.

🏢 Company: Health Care Global Enterprises (HCG Hospitals) 
🌐 Website: https://www.hcgoncology.com ;

👉 Role: Clinical Research Coordinator 
👉 Experience: 1–3 Years 
📍 Location: Vadodara, Gujarat 
🧾 Job Type: Full-Time, Permanent 
🏥 Department: Healthcare & Life Sciences 
🏢 Industry: Medical Services / Hospital 

🔧 Key Responsibilities:

• Oversee daily operations of multiple clinical trials 
• Maintain regulatory binders and study documentation 
• Ensure compliance with SOPs, study protocols, and GCP guidelines 
• Identify and recruit eligible study participants 
• Conduct informed consent procedures 
• Schedule and coordinate patient visits 
• Ensure participant safety throughout clinical studies 
• Record vital signs and ECGs 
• Collect and process blood and laboratory samples 
• Perform protocol-specific clinical procedures 
• Enter accurate clinical data into CRFs and EDC systems 
• Resolve data queries within required timelines 
• Maintain study records and source documentation 
• Prepare ethics and regulatory submissions 
• Ensure all research-related documents remain updated 
• Work closely with Principal Investigators (PIs) 
• Coordinate with sponsors, CROs, pharmacy teams, and monitors 
• Support monitoring visits, inspections, and audit readiness 

🛠 Required Skills:

• Knowledge of GCP guidelines and clinical trial protocols 
• Experience with CRF and EDC systems 
• Clinical trial coordination and study management skills 
• Patient recruitment and screening experience 
• Regulatory documentation and compliance knowledge 
• ECG and sample collection experience 
• Clinical data entry and documentation expertise 
• Strong communication and organizational skills 
• Ability to coordinate with multiple stakeholders and teams 

🎯 Preferred Skills / Requirements:

• B.Pharm, M.Pharm, or Pharm.D qualification 
• 1–3 years of experience in clinical research or clinical trial coordination 
• Experience in monitoring visit coordination and audit preparation 
• Strong understanding of regulatory and ethical standards in clinical research 

✨ Why Join Us?

• Exposure to oncology and advanced clinical research studies 
• Opportunity to work with experienced investigators and CROs 
• Career growth in clinical research operations 
• Stable full-time role in a reputed healthcare organization 
• Professional and learning-focused work environment 

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⚡ If you’re passionate about clinical trials, patient care, and research operations, this is a great opportunity to build your career with one of India’s leading healthcare organizations.