Are you searching for Clinical Research Coordinator Jobs in Raipur? ProClin Research is inviting applications from qualified professionals with 1โ3 years of clinical research experience. This is an excellent opportunity for candidates looking to build a rewarding career in the Clinical Research domain while working with a growing research organization.
Candidates with a Bachelor’s or Master’s degree in Life Sciences or Healthcare, along with a Clinical Research certification, are encouraged to apply.
If you’re looking for the latest Clinical Research Jobs in India, Clinical Research Coordinator vacancies, or Pharma Jobs for Clinical Research Professionals, this opportunity could be the right fit.
Job Overview
| Particular | Details |
|---|---|
| Company | ProClin Research |
| Job Role | Clinical Research Coordinator |
| Location | Raipur, Chhattisgarh |
| Experience | 1โ3 Years |
| Qualification | Bachelor’s or Master’s Degree in Scientific Discipline or Healthcare |
| Certification | Mandatory Clinical Research Certification |
| Industry | Clinical Research |
| Job Type | Full-Time |
Key Responsibilities
As a Clinical Research Coordinator, you will be responsible for:
- Coordinating clinical research activities and study execution.
- Ensuring compliance with ICH GCP E6(R3) guidelines.
- Maintaining study documentation and regulatory records.
- Supporting investigators during clinical trials.
- Assisting with participant recruitment and follow-up.
- Preparing reports and maintaining accurate clinical data.
- Coordinating with sponsors, ethics committees, and research teams.
- Managing study files using Microsoft Office applications.
- Ensuring compliance with NDCT Rules, 2019.
Required Qualifications
Applicants should possess:
- Bachelor’s or Master’s degree in a Scientific discipline or Healthcare.
- Mandatory Clinical Research Certification.
- 1โ3 years of Clinical Research experience.
- Strong understanding of ICH GCP E6(R3).
- Knowledge of New Drugs and Clinical Trials (NDCT) Rules, 2019.
- Excellent written and spoken English communication skills.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Strong documentation and organizational skills.
Preferred Skills
- Clinical Trial Coordination
- Clinical Documentation
- Regulatory Compliance
- GCP Compliance
- Investigator Site Coordination
- Good Clinical Practice
- Data Management
- Communication Skills
- Microsoft Office
- Team Collaboration
Why Join ProClin Research?
Joining ProClin Research offers an opportunity to:
- Build expertise in Clinical Research.
- Work on regulated clinical studies.
- Gain exposure to ICH GCP compliant research practices.
- Develop regulatory and documentation skills.
- Grow within a professional clinical research environment.
- Enhance career prospects in India’s expanding clinical research industry.
How to Apply
Interested candidates can share their updated CV via email.
Email: hr@proclinresearch.com
IF YOU ARE FRESHERS DONT APPLY OTHER WISE U WILL GET CALLS FROM THEIR INSTITUTES
Make sure your resume highlights:
- Clinical Research Certification
- Clinical Research Experience
- ICH GCP Knowledge
- NDCT Rules Knowledge
- Clinical Trial Coordination Experience