📍 Location: Kolkata & Bhubaneswar
🏥 Organization: OrciVita Sciences & Research Pvt. Ltd.
🧬 Position: Clinical Research Coordinator (CRC)
🕒 Experience Required: 0–3 Years (Freshers Can Apply)
📅 Date Posted: May 3, 2025
🎓 Qualification: B.Pharm, M.Pharm, Pharm.D, BSc, MSc, Nursing, Life Sciences
🧠 About OrciVita Sciences & Research Pvt. Ltd.
OrciVita is one of India’s top Site Management Organizations (SMOs). They play a critical role in conducting and managing global clinical trials by working closely with hospitals, investigators, and pharmaceutical companies.
With an expanding network across clinical research sites, OrciVita ensures high-quality patient recruitment, protocol compliance, and regulatory documentation — all vital for the success of medical studies.
This is an incredible opportunity for students, recent graduates, or early-career professionals interested in becoming part of the global clinical research ecosystem.
👨⚕️ Job Role: Clinical Research Coordinator (CRC)
The CRC role is pivotal in managing and executing day-to-day clinical trial activities at hospital-based research sites. As a CRC, you act as a bridge between the Principal Investigator (PI), sponsors, and clinical trial participants.
🔍 Key Responsibilities
✅ Trial Coordination
- Oversee the planning and execution of clinical trials at partnered hospitals
- Maintain clear communication between sponsors, CROs, investigators, and Ethics Committees
✅ Patient Management
- Assist in recruiting, screening, and consenting patients for clinical trials
- Schedule patient visits and follow-ups
✅ Documentation & Compliance
- Maintain accurate records like Informed Consent Forms (ICFs), Case Report Forms (CRFs), and source documents
- Ensure compliance with ICH-GCP guidelines and clinical protocol requirements
✅ Data Handling
- Enter clinical trial data into Electronic Data Capture (EDC) systems
- Resolve queries and track study progress in real-time
✅ Regulatory Support
- Liaise with Ethics Committees and provide all necessary study documentation
- Assist in drug supply management and ensure investigational products are handled properly
✅ Eligibility Criteria
| Criteria | Requirements |
|---|---|
| Education | B.Pharm, M.Pharm, Pharm.D, BSc, MSc in Life Sciences, or Nursing |
| Experience | 0 to 3 years in clinical research (Freshers encouraged) |
| Skillset | Strong in clinical documentation, EDC systems, and trial protocols |
| Knowledge | Familiarity with ICH-GCP guidelines is mandatory |
| Soft Skills | Communication, organizational, multitasking, and problem-solving abilities |
🌟 Why Choose OrciVita?
Working at OrciVita offers more than just a job—it’s a platform to launch your career in the fast-growing clinical research industry.
Top Reasons to Apply:
- 🌍 Global Trial Exposure: Get hands-on experience in international clinical studies
- 🏥 Hospital-Based Sites: Work directly at reputed hospital research centers
- 🧠 Multiple Therapeutic Areas: Oncology, cardiology, neurology, and more
- 👥 Mentorship Support: Learn under experienced Principal Investigators (PIs) and trial managers
- 📈 Career Growth: Move up the ladder from CRC to CRA, project coordinator, or regulatory associate
- 💰 Good Salary: Competitive CTC with medical and professional development perks
🗂️ Work Environment
- Hospital-based and site-facing role
- Weekday work with occasional weekend trial coordination
- Real-world exposure to patients, sponsors, and global study teams
- Hybrid learning model: On-site execution + periodic training
🧭 Career Path After CRC Role
| Level | Career Role |
|---|---|
| Entry | Clinical Research Coordinator |
| Mid | Clinical Research Associate (CRA) |
| Advanced | Site Manager / Clinical Project Coordinator |
| Specialist | Regulatory Affairs / Pharmacovigilance Officer |
📝 Application Process
How to Apply:
📧 Send your updated CV to: hrorcivita@gmail.com
📝 Subject Line:
- If applying for Kolkata: “CRC Application – Kolkata”
- If applying for Bhubaneswar: “CRC Application – Bhubaneswar”
📌 Pro Tip: Mention your location preference and availability clearly in the email body to increase your selection chances.
🧾 Summary Snapshot
| Detail | Info |
|---|---|
| Job Role | Clinical Research Coordinator |
| Company | OrciVita Sciences & Research Pvt. Ltd. |
| Locations | Kolkata & Bhubaneswar |
| Qualification | B.Pharm, M.Pharm, Pharm.D, BSc, MSc, Nursing |
| Experience | 0–3 Years |
| Salary | Competitive (Depends on Interview) |
| Skills | Clinical documentation, patient management, data entry, compliance |
| Work Model | On-site hospital work |
| Hiring Type | Immediate |
🔚 Final Thoughts
This is a golden opportunity for freshers or experienced clinical professionals looking to gain direct experience in trial site coordination, documentation, and patient engagement. With exposure to global protocols and therapeutic areas, you’ll build a strong foundation for a rewarding career in clinical research, CROs, or pharma companies.
If you’re passionate about contributing to medical research, patient safety, and innovation, take the first step with OrciVita.
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