This opportunity is suitable for fresh graduates who want to begin a career in clinical research and experienced candidates looking to continue in trial coordination roles.
Job Overview
| Particulars | Details |
|---|---|
| Position | Clinical Research Coordinator (CRC) / Intern Clinical Research Coordinator |
| Company | Metta Clinical Research is a clinical research organization focused on supporting clinical trial activities, research operations, and healthcare studies |
| Location | Nagpur, Maharashtra |
| Job Type | Full-Time |
| Experience | 0 - 1 years |
| Category / Department | CDM |
| Application Mode |
π’ About Metta Clinical Research is a clinical research organization focused on supporting clinical trial activities, research operations, and healthcare studies
Metta Clinical Research is a clinical research organization focused on supporting clinical trial activities, research operations, and healthcare studies.
The organization provides opportunities for professionals and fresh graduates to gain practical exposure in clinical research coordination, regulatory documentation, patient management, and trial operations.
π‘ Editor's Note / Preparation Tip
This recruitment update is created to help Life Science and pharmacy professionals explore opportunities in the clinical research field. Candidates should verify job details, eligibility criteria, and interview information through official company communication before applying.
π Job Description
Metta Clinical Research Hiring Clinical Research Coordinator | Freshers & Experienced Jobs Nagpur
Company Name: Metta Clinical Research
Job Role: Clinical Research Coordinator (CRC) / Intern Clinical Research Coordinator
Department: Clinical Research
Location: Nagpur, Maharashtra
Employment Type: Full-Time
Work Mode: On-site
Experience: Freshers & Experienced Candidates
Available Positions
1. Clinical Research Coordinator (CRC) β Experienced
Eligibility:
β’ Life Science Graduate / B.Pharm / M.Pharm
β’ Minimum 1 year experience in clinical trials
β’ Knowledge of clinical research documentation
β’ Patient coordination experience preferred
2. Intern Clinical Research Coordinator (Intern CRC)
Eligibility:
β’ Life Science Graduate
β’ B.Pharm graduates
β’ Freshers can apply
β’ Clinical Research certification/diploma is not mandatory
Why Join Metta Clinical Research?
β’ Excellent opportunity for clinical research freshers
β’ Practical exposure to clinical trials
β’ Learning from experienced research professionals
β’ Understanding of regulatory documentation
β’ Career growth opportunities in clinical research
β’ Professional and supportive work environment
Salary Details (Estimated)
Intern Clinical Research Coordinator:
βΉ2.2 LPA β βΉ3.2 LPA
Clinical Research Coordinator (1+ Year Experience):
βΉ3.6 LPA β βΉ5.8 LPA
Salary may vary based on qualification, skills, and interview performance.
How to Apply
Interested candidates can send their updated resume to:
Email: info@mettaclinical.com
Subject Line:
For Experienced CRC:
βExperienced CRC Application β Nagpurβ
For Intern CRC:
βIntern CRC Application β Nagpurβ
Start your clinical research career with Metta Clinical Research and gain valuable industry experience.
π― Key Responsibilities
- β Coordinate clinical research studies
- β Support patient screening and enrollment activities
- β Maintain clinical trial documentation and regulatory records
- β Assist investigators during study procedures
- β Schedule patient visits and follow-ups
- β Ensure compliance with GCP, SOPs, and study protocols
- β Collect and manage clinical trial data
- β Coordinate with sponsors, CROs, and ethics committees
- β Support monitoring visits and audit activities
- β Maintain accurate study-related records
π‘ Required Qualifications & Skills
Frequently Asked Questions
Q1: Who can apply for the Intern CRC position?
Freshers with Life Science or B.Pharm qualifications can apply.
Q2: Is a Clinical Research course mandatory?
No, a clinical research certification or diploma is not mandatory for the Intern CRC role.
Q3: What experience is required for CRC?
Experienced CRC candidates should have at least 1 year of clinical trial experience.
Q4: Where is the job location?
The position is based in Nagpur, Maharashtra.
Q5: What skills are useful for this role?
Clinical documentation, communication skills, patient coordination, and understanding of clinical trial processes are preferred.
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