SiteInsight Research is inviting applications for the position of Clinical Research Coordinator at its Bhopal location. This is an excellent opportunity for professionals with experience in clinical research, clinical trials, GCP, ICH guidelines, and research documentation. Candidates with qualifications in Life Sciences, Pharmacy, Nursing, or related disciplines looking to build a rewarding career in clinical research are encouraged to apply.
Working at SiteInsight Research provides exposure to patient-centered clinical trials, regulatory compliance, protocol implementation, and collaboration with investigators, sponsors, and healthcare professionals. If you are passionate about advancing medical research while ensuring participant safety and data integrity, this opportunity is worth considering.
SiteInsight Research Recruitment 2026 – Overview
| Job Details | Information |
|---|---|
| Company | SiteInsight Research |
| Position | Clinical Research Coordinator |
| Job Type | Full-Time |
| Work Mode | On-Site |
| Location | Bhopal, Madhya Pradesh |
| Qualification | Life Sciences, Pharmacy, Nursing or Related Degree |
| Experience | Clinical Research Experience Preferred |
| Industry | Clinical Research Organization (CRO) |
| Application Mode | |
| Projects@siteinsightresearch.com |
About SiteInsight Research
SiteInsight Research is a clinical research organization dedicated to conducting high-quality, patient-focused clinical trials across multiple therapeutic areas. The organization collaborates with investigators, sponsors, and healthcare professionals to ensure every study meets international ethical, scientific, and regulatory standards.
The company emphasizes:
- Patient safety
- Regulatory compliance
- Accurate clinical data
- Professional development
- Collaborative work culture
- High-quality clinical trial execution
Job Responsibilities
As a Clinical Research Coordinator, you will be responsible for coordinating day-to-day clinical trial activities while ensuring compliance with study protocols and regulatory requirements.
Key Responsibilities
- Coordinate participant screening and enrollment
- Schedule and manage clinical study visits
- Obtain and document informed consent accurately
- Maintain source documents and Case Report Forms (CRFs)
- Perform timely data entry and resolve data queries
- Implement study protocols according to GCP guidelines
- Maintain study supplies and essential documentation
- Handle ethics committee and regulatory documentation
- Coordinate with investigators, sponsors, and clinical monitors
- Track adverse events and participant safety
- Ensure protocol compliance throughout the study
- Maintain high standards of research documentation
Eligibility Criteria
Candidates should possess:
- Degree in Life Sciences
- B.Pharm
- M.Pharm
- B.Sc
- M.Sc
- Nursing or other relevant healthcare qualification
Required Skills
Applicants should have knowledge and experience in:
- Clinical Research
- Clinical Trial Coordination
- Informed Consent Process
- Study Protocol Implementation
- Good Clinical Practice (GCP)
- ICH Guidelines
- Research Documentation
- Case Report Forms (CRFs)
- Source Documentation
- Data Management
- Regulatory Documentation
- Ethics Committee Coordination
- Adverse Event Reporting
- Strong Communication Skills
- Excellent Organizational Skills
- Attention to Detail
- Multitasking Abilities
Why Join SiteInsight Research?
Joining SiteInsight Research offers several career advantages:
- Work on patient-centered clinical trials
- Exposure to international research standards
- Collaborative research environment
- Career growth in Clinical Research
- Opportunity to work with investigators and sponsors
- Continuous professional learning
- Experience with regulatory and ethics processes
- Contribution to medical innovation and patient care
How to Apply
Interested candidates can send their updated CV to:
📧 Email: Projects@siteinsightresearch.com