Health Care Global Enterprises is hiring for the position of Clinical Research Coordinator in Vadodara, Gujarat. This opportunity is ideal for candidates with 1โ3 years of clinical research experience and qualifications such as B.Pharm, M.Pharm, or Pharm.D.
Candidates with experience in clinical trial coordination, regulatory compliance, patient recruitment, CRF data entry, and study management are encouraged to apply for this healthcare and clinical research job opening.
Job Overview
- Job Title: Clinical Research Coordinator
- Company: Health Care Global Enterprises
- Location: Vadodara
- Experience Required: 1โ3 Years
- Qualification: B.Pharm, M.Pharm, Pharm.D
- Job Type: Full-Time, Permanent
- Department: Healthcare & Life Sciences
- Industry: Medical Services / Hospital
Key Responsibilities
The selected candidate will manage and coordinate clinical research activities while ensuring compliance with regulatory and ethical standards.
Study Management
- Oversee daily operations of multiple clinical trials
- Maintain regulatory binders and study documentation
- Ensure compliance with SOPs, protocols, and GCP guidelines
Participant Management
- Identify and recruit eligible study participants
- Conduct informed consent procedures
- Schedule and coordinate patient visits
- Ensure participant safety during the clinical study
Clinical Procedures
- Record vital signs and ECGs
- Collect and process blood and laboratory samples
- Perform protocol-specific clinical procedures
Data Management
- Enter accurate data into CRFs and EDC systems
- Resolve data queries within timelines
- Maintain study records and source documentation
Regulatory Compliance
- Prepare ethics and regulatory submissions
- Ensure all research-related documents remain updated
Coordination & Communication
- Work closely with Principal Investigators (PIs)
- Coordinate with sponsors, CROs, pharmacy teams, and monitors
- Support monitoring visits and audit readiness
Eligibility Criteria
Candidates applying for this Clinical Research Coordinator job should have:
- B.Pharm, M.Pharm, or Pharm.D qualification
- 1โ3 years of experience in clinical research or clinical trial coordination
- Knowledge of:
- GCP guidelines
- Clinical trial protocols
- Regulatory documentation
- CRF and EDC systems
- Strong communication and organizational skills
Preferred Skills
- Clinical trial coordination
- Patient recruitment and screening
- Regulatory compliance
- ECG and sample collection
- Clinical data entry
- Monitoring visit coordination
- Clinical research documentation
Why Join Health Care Global Enterprises?
Working with Health Care Global Enterprises offers professionals an opportunity to gain exposure in advanced clinical research and patient-focused healthcare operations.
Employee Benefits
- Exposure to oncology and clinical research studies
- Opportunity to work with experienced investigators and CROs
- Career growth in clinical research operations
- Stable full-time healthcare role
- Professional learning environment
How to Apply
