CtrialPro is inviting applications for the position of Clinical Research Coordinator (CRC) for freshers and candidates with up to 1 year of experience. This is an excellent opportunity for candidates from B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, Biotechnology, Nursing, and Allied Health Sciences backgrounds to begin a rewarding career in the fast-growing clinical research industry.
As a Clinical Research Coordinator, you will work alongside Principal Investigators, sponsors, Clinical Research Associates (CRAs), ethics committees, and patients to ensure clinical studies are conducted in compliance with ICH-GCP guidelines, regulatory requirements, and study protocols. If you aspire to build a long-term career in clinical research, pharmacovigilance, regulatory affairs, or clinical operations, this opportunity is an ideal starting point.
Clinical Research Coordinator Vacancy 2026 – Job Overview
| Particulars | Details |
|---|---|
| Company | CtrialPro |
| Job Title | Clinical Research Coordinator (CRC) |
| Location | Kolkata, West Bengal |
| Experience | 0–1 Year (Freshers Eligible) |
| Qualification | B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc Life Sciences, Biotechnology, Nursing, Allied Health Sciences |
| Industry | Clinical Research / Healthcare / Pharmaceuticals |
| Employment Type | Full-Time |
| Application Mode | |
| hr@ctrialpro.in |
About the Clinical Research Coordinator Role
The Clinical Research Coordinator (CRC) plays a vital role in ensuring the smooth execution of clinical trials while maintaining compliance with international quality and regulatory standards. The position provides practical exposure to patient management, clinical documentation, regulatory submissions, clinical data management, monitoring support, and investigator coordination.
This opportunity is highly suitable for candidates planning careers in:
- Clinical Research
- Clinical Operations
- Clinical Trial Management
- Clinical Data Management
- Pharmacovigilance
- Regulatory Affairs
- Clinical Trial Monitoring
Key Responsibilities
Selected candidates will be responsible for:
- Assist investigators in conducting clinical trials according to ICH-GCP guidelines.
- Coordinate patient screening and recruitment activities.
- Explain and document Informed Consent Forms (ICF).
- Schedule and coordinate patient visits.
- Maintain Investigator Site Files (ISF).
- Manage Trial Master Files (TMF/eTMF).
- Maintain accurate source documentation.
- Enter study data into CRFs and Electronic Data Capture (EDC) systems.
- Resolve clinical data queries.
- Coordinate with sponsors, CROs, and Clinical Research Associates.
- Support monitoring visits and regulatory audits.
- Prepare Ethics Committee submission documents.
- Ensure protocol compliance throughout the study.
- Track adverse events and protocol deviations.
- Assist with study close-out activities.
Educational Qualifications
Candidates with any of the following qualifications are eligible:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Nursing
- Allied Health Sciences
Experience Required
- Freshers can apply.
- 0–12 months of experience preferred.
- Internship experience in clinical research is an added advantage.
Required Skills
Ideal candidates should possess:
- Basic understanding of Clinical Trials
- ICH-GCP knowledge
- Good Documentation Practices (GDP)
- MS Office proficiency
- Strong communication skills
- Teamwork and collaboration
- Attention to detail
- Patient interaction skills
- Time management
- Clinical data management knowledge
Preferred Qualifications
Candidates having the following qualifications will receive preference:
- Clinical Research Certification
- PG Diploma in Clinical Research
- GCP Certification
- Internship in hospitals or CROs
- Knowledge of NDCT Rules
- Exposure to EDC software
Career Growth Opportunities
A Clinical Research Coordinator can progress to positions such as:
- Clinical Research Associate (CRA)
- Senior Clinical Research Coordinator
- Clinical Trial Associate
- Clinical Operations Executive
- Clinical Data Manager
- Regulatory Affairs Associate
- Pharmacovigilance Associate
- Medical Writer
- Project Coordinator
- Study Lead
Why Join CtrialPro?
Working as a Clinical Research Coordinator provides numerous career advantages:
- Excellent career growth opportunities
- High demand across CROs and pharmaceutical companies
- Exposure to international clinical trials
- Hands-on experience in clinical operations
- Competitive salary packages
- Continuous professional learning
- Opportunity to work with experienced investigators and sponsors
Salary
Expected annual salary:
- Freshers: ₹2.5–4.5 LPA
- 0–1 Year Experience: ₹3.5–5.5 LPA
Salary may vary depending on qualifications, experience, and company policies.
How to Apply
Interested candidates should:
- Update their latest resume.
- Mention all relevant certifications and internship experience.
- Use the email subject:
Application for Clinical Research Coordinator – Kolkata – Your Name
Send your updated CV to:
Email: hr@ctrialpro.in