Are you searching for Clinical Research Coordinator jobs in Kolkata? Here’s an excellent opportunity for freshers and candidates with up to 1 year of experience to start their career in the rapidly growing clinical research industry. If you have qualifications in B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, or Nursing, this could be the perfect opportunity to gain hands-on experience in clinical trials and patient management.
Clinical Research Coordinators (CRCs) are an essential part of every clinical trial. They work closely with Principal Investigators, sponsors, Clinical Research Associates (CRAs), ethics committees, and patients to ensure studies are conducted according to international regulatory standards.
📌 Job Overview
| Job Details | Information |
|---|---|
| Position | 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 |
| Industry | Clinical Research / Healthcare / Pharmaceuticals |
| Employment Type | Full-Time |
| Application Mode | |
| Email ID | hr@ctrialpro.in |
About the Clinical Research Coordinator Role
Clinical Research Coordinators ensure smooth execution of clinical studies while maintaining compliance with ICH-GCP guidelines, regulatory requirements, and study protocols.
As a CRC, you’ll gain valuable experience in patient recruitment, documentation, clinical data management, regulatory submissions, and coordination with sponsors and investigators.
This position offers an excellent learning platform for individuals planning long-term careers in:
- Clinical Research
- Clinical Operations
- Clinical Data Management
- Pharmacovigilance
- Regulatory Affairs
- Clinical Trial Monitoring
Key Responsibilities
Selected candidates will be responsible for:
- Assisting investigators in conducting clinical trials according to ICH-GCP.
- Coordinating patient screening and recruitment.
- Explaining and documenting Informed Consent Forms (ICF).
- Scheduling patient visits.
- Maintaining Investigator Site Files (ISF).
- Managing Trial Master Files (TMF/eTMF).
- Maintaining source documents.
- Entering data into CRFs and Electronic Data Capture (EDC) systems.
- Resolving clinical data queries.
- Coordinating with sponsors, CROs and Clinical Research Associates.
- Supporting monitoring visits and regulatory audits.
- Preparing documentation for Ethics Committee submissions.
- Maintaining protocol compliance.
- Tracking adverse events and protocol deviations.
- Supporting study close-out activities.
Educational Qualification
Candidates should possess any of the following qualifications:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Nursing
- Allied Health Sciences
Experience Required
- Freshers are eligible.
- 0–12 months experience preferred.
- Internship experience in clinical research will be an advantage.
Skills Required
Ideal candidates should possess:
- Basic understanding of Clinical Trials
- ICH-GCP knowledge
- Good Documentation Practices
- MS Office proficiency
- Communication skills
- Teamwork
- Attention to detail
- Patient interaction skills
- Time management
- Data management skills
Preferred Qualifications
Candidates with the following will have an added advantage:
- Clinical Research Certification
- PG Diploma in Clinical Research
- GCP Certification
- Internship at hospitals or CROs
- Knowledge of NDCT Rules
- Exposure to EDC software
Career Growth
Starting as a Clinical Research Coordinator can open opportunities for 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 Choose Clinical Research?
The Indian clinical research industry is growing rapidly due to increasing clinical trials, pharmaceutical innovation, and global outsourcing.
Benefits include:
- Excellent career growth
- High demand for skilled professionals
- Opportunities in multinational CROs
- International exposure
- Competitive salary packages
- Continuous learning opportunities
Salary Expectations
Approximate salary ranges:
- Freshers: ₹2.5–4.5 LPA
- 1 Year Experience: ₹3.5–5.5 LPA
(Salary depends on company policies and candidate experience.)
How to Apply
Interested candidates should:
- Update their resume.
- Mention relevant certifications and internships.
- Use the subject line:
Application for Clinical Research Coordinator – Kolkata – Your Name
- Email your updated CV to:
Frequently Asked Questions (FAQs)
Is this job open for freshers?
Yes. Fresh graduates with relevant educational qualifications are encouraged to apply.
Is GCP Certification mandatory?
No. However, having GCP certification or Clinical Research training will improve your chances.
Can Life Science graduates apply?
Yes. Candidates from Life Sciences, Biotechnology, Pharmacy, Nursing, and Allied Health Sciences are eligible.
Is prior CRC experience compulsory?
No. Freshers and candidates with internship experience can also apply.
What skills are most important?
Documentation, communication, ICH-GCP knowledge, patient coordination, and MS Office skills.
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