Are you a Life Sciences or Pharmacy graduate searching for your first opportunity in the clinical research industry? Here’s some exciting news! OrciVita has announced its latest recruitment drive for the position of Clinical Research Coordinator (CRC) in Ranchi and Kolkata.
This opportunity is ideal for fresh graduates who want to build a rewarding career in clinical trials, pharmaceutical research, and healthcare management. If you’re passionate about medical research, patient care, and contributing to the development of new medicines, this could be the perfect career opportunity for you.
Clinical research is among the fastest-growing industries in India, and starting your career as a Clinical Research Coordinator offers excellent learning opportunities, professional growth, and long-term career prospects.
Whether you hold a B.Sc, M.Sc in Life Sciences, or B.Pharm degree, this recruitment drive could be your gateway into one of the most promising healthcare careers.
๐ Job Overview
| Particular | Details |
|---|---|
| Company | OrciVita |
| Position | Clinical Research Coordinator (CRC) |
| Job Type | Full-Time |
| Experience | Freshers & Experienced |
| Qualification | B.Sc, M.Sc (Life Sciences), B.Pharm |
| Job Location | Ranchi & Kolkata |
| Industry | Clinical Research |
| Application Mode |
๐ข About OrciVita
OrciVita is an emerging clinical research organization dedicated to supporting hospitals, pharmaceutical companies, and healthcare institutions in conducting ethical and high-quality clinical trials.
The organization focuses on maintaining international standards while ensuring patient safety, regulatory compliance, and accurate clinical documentation throughout every research project.
Working at OrciVita gives fresh graduates an opportunity to learn directly from experienced investigators and clinical professionals while gaining practical industry exposure.
๐ฌ What Does a Clinical Research Coordinator Do?
A Clinical Research Coordinator (CRC) plays a vital role in ensuring that clinical trials run smoothly from beginning to end.
Working under the supervision of the Principal Investigator (PI), the CRC manages patient coordination, study documentation, regulatory paperwork, scheduling, and communication between sponsors and investigators.
Some of the major responsibilities include:
- Coordinating clinical trial activities
- Maintaining trial documentation
- Scheduling participant visits
- Managing informed consent documentation
- Recording clinical data accurately
- Supporting monitoring visits
- Ensuring compliance with Good Clinical Practice (GCP)
- Assisting investigators during audits and inspections
Clinical Research Coordinators are considered the backbone of every successful clinical trial.
๐ Job Locations
OrciVita is currently hiring for the following locations:
- ๐ Ranchi (Jharkhand)
- ๐ Kolkata (West Bengal)
Important: Preference will be given to candidates who are currently residing in Ranchi or Kolkata, as this is an on-site position.
๐ Educational Qualification
Candidates should possess any of the following qualifications:
- B.Sc Life Sciences
- M.Sc Life Sciences
- B.Pharm
Eligible specializations include:
- Biotechnology
- Microbiology
- Biochemistry
- Zoology
- Botany
- Genetics
- Biomedical Sciences
- Pharmacy
Fresh graduates who have recently completed their degree are encouraged to apply.
๐จโ๐ Experience Required
- Freshers can apply
- Candidates with internship experience in hospitals or clinical research organizations will have an added advantage.
- Previous exposure to GCP or clinical documentation is beneficial but not mandatory.
โ Skills Required
The ideal candidate should possess:
- Excellent communication skills
- Good documentation abilities
- Strong organizational skills
- Basic computer knowledge
- MS Office proficiency
- Attention to detail
- Teamwork abilities
- Time management skills
- Basic understanding of clinical research
- Knowledge of GCP guidelines (preferred)
๐ Key Responsibilities
As a Clinical Research Coordinator, your daily responsibilities may include:
๐ฉบ Patient Coordination
- Schedule participant visits
- Coordinate appointments
- Explain study procedures
- Support informed consent process
๐ Clinical Documentation
Maintain important study documents such as:
- Source documents
- Case Report Forms (CRFs)
- Trial Master Files
- Regulatory documents
- Patient records
๐ป Data Management
- Record patient information
- Verify clinical data
- Maintain electronic records
- Resolve data discrepancies
โ๏ธ Regulatory Compliance
Ensure that every clinical trial follows:
- Good Clinical Practice (GCP)
- ICH Guidelines
- Institutional Ethics Committee requirements
- Sponsor protocols
- Regulatory authority guidelines
๐ Investigational Product Management
Assist in:
- Drug accountability
- Storage documentation
- Temperature monitoring
- Inventory management
๐ Communication
Coordinate regularly with:
- Principal Investigator
- Clinical Research Associates (CRA)
- Study Sponsors
- Ethics Committee
- Hospital Staff
- Patients
๐ฐ Salary
Although the company has not officially disclosed the salary package, candidates can expect industry-standard compensation.
Approximate salary range:
- Freshers: โน2.5 โ โน4.5 LPA
- Experienced Candidates: Higher based on experience
Additional benefits may include:
- Professional training
- Career development
- Exposure to global clinical trials
- Learning opportunities
- Networking with healthcare professionals
๐ Career Growth
Starting as a Clinical Research Coordinator opens doors to several high-paying careers such as:
- Clinical Research Associate (CRA)
- Senior CRC
- Clinical Trial Associate
- Clinical Data Coordinator
- Clinical Data Manager
- Regulatory Affairs Executive
- Medical Writer
- Project Coordinator
- Clinical Project Manager
With experience, professionals can also move into multinational pharmaceutical companies and CROs.
๐ Why Join OrciVita?
Some advantages of joining include:
- Freshers are welcome
- Industry exposure
- Work with experienced investigators
- Clinical research training
- Career advancement opportunities
- Ethical work environment
- Real-time clinical trial experience
๐ฉ How to Apply?
Interested candidates should follow these steps:
Step 1
Prepare an updated resume highlighting:
- Educational qualifications
- Internship experience (if any)
- Certifications
- Projects
- Skills
Step 2
Write a professional email mentioning:
- Current location
- Qualification
- Contact details
- Availability
Step 3
Send your resume to the official recruitment email IDs.
๐ง Apply Now
Email your updated CV to:
๐ฉ contact@orcivita.com
๐ฉ hrorcivita@gmail.com
โ๏ธ HR Contact: +91 9147310090
Subject Line Suggestion:
Application for Clinical Research Coordinator โ Ranchi/Kolkata
๐ Documents Required
Keep the following documents ready:
- Updated Resume
- Educational Certificates
- Identity Proof
- Passport-size Photograph
- Internship Certificates (if available)
- Experience Certificates (if applicable)
๐ก Tips to Increase Your Selection Chances
- Create an ATS-friendly resume.
- Mention clinical research certifications.
- Highlight internships and projects.
- Improve communication skills.
- Learn the basics of Good Clinical Practice (GCP).
- Revise clinical research fundamentals before the interview.
โ Frequently Asked Questions (FAQs)
1. Can freshers apply?
Yes. Fresh graduates are encouraged to apply.
2. What qualifications are accepted?
B.Sc, M.Sc in Life Sciences, and B.Pharm.
3. Is experience mandatory?
No. Freshers are eligible.
4. Where are the job locations?
Ranchi and Kolkata.
5. Is this a work-from-home job?
No. It is an on-site Clinical Research Coordinator role.
6. How can I apply?
Send your updated resume to:
๐ Recommended Jobs
You may also like:
- IQVIA Lab Centralized Project Coordinator Jobs 2026
- FDHS Project Coordinator Recruitment 2026
- ICON plc Clinical Data Coordinator Recruitment
- Thermo Fisher Scientific Clinical Data Management Jobs
- JAMP India Regulatory Affairs Walk-In Drive
(Replace these with your actual internal links on JobsOnTheWay.com.)
๐ข Final Words
If you are passionate about clinical research and looking to start your professional journey with a growing healthcare organization, this Clinical Research Coordinator opportunity at OrciVita is worth considering. Fresh graduates from Life Sciences and Pharmacy backgrounds have an excellent chance to gain valuable industry exposure while working on real-world clinical trials.
Since openings may close once suitable candidates are selected, interested applicants are advised to submit their resumes as early as possible.
SEO Meta Description
Apply for OrciVita Careers 2026! Freshers can apply for Clinical Research Coordinator (CRC) jobs in Ranchi and Kolkata. B.Sc, M.Sc Life Sciences & B.Pharm graduates eligible. Apply now.
๐ Related Job Opportunities
- ICON plc Hiring Clinical Data Coordinator I (CDC I) | Hybrid Clinical Data Management Job Opportunity in India 2026
- JAMP India Pharmaceuticals Walk-In Drive 2026 | Regulatory Affairs (eCTD) Career Opportunities in Ahmedabad
- Thermo Fisher Scientific Hiring Clinical Data Management Professionals | Clinical Data Associate & Senior Clinical Data Associate Jobs 2026
- Levim Lifetech Pvt. Ltd. Freshers Hiring 2026 | Junior Research Associate (R&D) | Life Science & Biotechnology Graduates Apply Now
- IQVIA Patent Analyst Recruitment 2026 | Hybrid Patent Intelligence Jobs in Gurgaon for M.Pharm & Biotechnology Professionals
- Eris Lifesciences Hiring New Product Development Executive in Mumbai | PharmD & MBA Professionals Can Apply