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 |
🏢 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.
💡 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.
📝 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) – Experienced
Eligibility:
• Life Science Graduate / B.Pharm / M.Pharm
• Minimum 1 year experience in clinical trials
• Knowledge of clinical research documentation
• Patient coordination experience preferred
2. Intern Clinical Research Coordinator (Intern CRC)
Eligibility:
• Life Science Graduate
• B.Pharm graduates
• Freshers can apply
• Clinical Research certification/diploma is not mandatory
Why Join Metta Clinical Research?
• Excellent opportunity for clinical research freshers
• Practical exposure to clinical trials
• Learning from experienced research professionals
• Understanding of regulatory documentation
• Career growth opportunities in clinical research
• Professional and supportive work environment
Salary Details (Estimated)
Intern Clinical Research Coordinator:
₹2.2 LPA – ₹3.2 LPA
Clinical Research Coordinator (1+ Year Experience):
₹3.6 LPA – ₹5.8 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:
“Experienced CRC Application – Nagpur”
For Intern CRC:
“Intern CRC Application – Nagpur”
Start your clinical research career with Metta Clinical Research and gain valuable industry experience.
🎯 Key Responsibilities
- ✓ Coordinate clinical research studies
- ✓ Support patient screening and enrollment activities
- ✓ Maintain clinical trial documentation and regulatory records
- ✓ Assist investigators during study procedures
- ✓ Schedule patient visits and follow-ups
- ✓ Ensure compliance with GCP, SOPs, and study protocols
- ✓ Collect and manage clinical trial data
- ✓ Coordinate with sponsors, CROs, and ethics committees
- ✓ Support monitoring visits and audit activities
- ✓ Maintain accurate study-related records
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Clinical Research Coordinator (CRC) / Intern Clinical Research Coordinator role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
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.
Share This Job
🛡️ Safety Disclaimer: JobPortalConnect curates official listings for informational purposes. Genuine recruiters will never ask you for processing fees, training payments, or security deposits. If you spot suspicious activity, copyright issues, or wish to request the removal of this listing, please report it to us immediately at contact.jobportalconnect@gmail.com.