Kickstart Your Clinical Research Career with Shivensis Research
Are you a Life Sciences, Pharmacy, or Biotechnology graduate looking for an exciting opportunity to enter the fast-growing clinical research industry? Do you aspire to work directly with clinical trials, patient care, and medical innovations that help shape the future of healthcare? If yes, then this opportunity from Shivensis Research could be the perfect starting point for your professional journey.
Shivensis Research has announced recruitment for the position of Clinical Research Coordinator (CRC) for its Delhi and Faridabad locations. The organization is inviting applications from fresh graduates, interns, and early-career professionals who want to gain practical experience in clinical trial management and research operations.
Clinical research is one of the fastest-growing sectors in the pharmaceutical and healthcare industry. As global pharmaceutical companies continue to invest heavily in drug development, the demand for skilled Clinical Research Coordinators is increasing significantly across India.
If you are searching for Clinical Research Coordinator Jobs 2026, CRC Fresher Jobs in Delhi, or Clinical Research Jobs for Life Science Graduates, this opportunity deserves your attention.
About Shivensis Research
Shivensis Research is actively involved in clinical research activities and provides support for clinical studies conducted according to international quality and regulatory standards. The organization focuses on maintaining ethical practices, patient safety, and compliance with Good Clinical Practice (GCP) guidelines.
The company offers young professionals an excellent platform to gain exposure to real-world clinical trials while working alongside experienced investigators, healthcare professionals, and research teams.
For freshers who want practical industry exposure, Shivensis Research provides an environment where learning and career growth go hand in hand.
Job Overview
| Particulars | Details |
|---|---|
| Company Name | Shivensis Research |
| Position | Clinical Research Coordinator (CRC) |
| Job Type | Full-Time |
| Vacancies | 02 Positions |
| Location | Delhi & Faridabad |
| Experience | Freshers / Interns Eligible |
| Salary | Competitive Salary/Stipend |
| Industry | Clinical Research |
| Language Requirement | Hindi & English |
Who Can Apply?
Candidates from Life Sciences, Pharmacy, and Biotechnology backgrounds are encouraged to apply.
Eligible Qualifications
Pharmacy Candidates
- B.Pharm
- M.Pharm
- Pharm.D
Life Sciences Candidates
- B.Sc Biology
- B.Sc Microbiology
- B.Sc Biochemistry
- B.Sc Zoology
- M.Sc Life Sciences
- M.Sc Microbiology
- M.Sc Biochemistry
Biotechnology Candidates
- B.Sc Biotechnology
- M.Sc Biotechnology
- B.Tech Biotechnology
- M.Tech Biotechnology
Freshers with strong academic knowledge and a passion for clinical research are highly encouraged to apply.
What is a Clinical Research Coordinator?
A Clinical Research Coordinator (CRC) plays a vital role in managing clinical trial activities at research sites. CRCs ensure that studies are conducted according to approved protocols, ethical guidelines, and regulatory requirements.
They act as the bridge between:
- Investigators
- Study Participants
- Sponsors
- Contract Research Organizations (CROs)
- Ethics Committees
- Regulatory Authorities
Without Clinical Research Coordinators, the successful execution of clinical trials would be nearly impossible.
Key Responsibilities of a Clinical Research Coordinator
1. Clinical Trial Coordination
The CRC manages daily operational activities related to ongoing clinical studies.
Responsibilities include:
- Scheduling patient visits
- Managing study documentation
- Coordinating investigator meetings
- Tracking study timelines
2. Patient Recruitment and Screening
One of the most important responsibilities involves identifying suitable participants for clinical trials.
Tasks include:
- Screening potential participants
- Verifying eligibility criteria
- Scheduling enrollment visits
- Maintaining participant records
3. Informed Consent Process
Clinical Research Coordinators assist investigators during the informed consent process.
Responsibilities include:
- Explaining study procedures
- Discussing benefits and risks
- Ensuring participant understanding
- Maintaining proper documentation
This process is essential for protecting participant rights and maintaining ethical compliance.
4. Maintaining Regulatory Compliance
Clinical trials are governed by strict regulations.
CRCs help ensure compliance with:
- Good Clinical Practice (GCP)
- Institutional SOPs
- Ethics Committee requirements
- Regulatory authority guidelines
- Study protocols
5. Documentation and Record Management
Accurate documentation is critical in clinical research.
CRC responsibilities include:
- Maintaining Trial Master Files
- Updating Case Report Forms (CRFs)
- Managing source documents
- Filing regulatory records
- Preparing study reports
6. Safety Reporting
Participant safety is the highest priority in clinical research.
CRCs monitor:
- Adverse Events (AEs)
- Serious Adverse Events (SAEs)
- Protocol deviations
- Safety concerns
All incidents must be documented and reported according to regulatory timelines.
7. Coordination with Stakeholders
Clinical Research Coordinators communicate regularly with:
- Principal Investigators
- Sponsors
- CRO Teams
- Ethics Committees
- Monitoring Teams
Strong communication skills are essential for success in this role.
8. Site Monitoring Support
Clinical trial sites are regularly visited by monitors and auditors.
CRCs assist during:
- Site Initiation Visits (SIV)
- Interim Monitoring Visits (IMV)
- Close-Out Visits (COV)
- Regulatory Inspections
Their role ensures that all required documents and records are readily available.
Why Choose Clinical Research as a Career?
The clinical research industry offers excellent growth opportunities and long-term career stability.
Rapid Industry Growth
India has become a major hub for global clinical research activities. As pharmaceutical companies expand their clinical development programs, demand for qualified professionals continues to rise.
High Learning Opportunities
Working as a CRC allows freshers to gain hands-on exposure to:
- Clinical trial operations
- Regulatory compliance
- Patient management
- Research documentation
- Healthcare systems
Diverse Career Options
After gaining experience as a CRC, professionals can progress into various roles:
- Clinical Research Associate (CRA)
- Senior CRC
- Clinical Trial Assistant (CTA)
- Clinical Trial Manager
- Clinical Project Manager
- Regulatory Affairs Associate
- Pharmacovigilance Associate
- Quality Assurance Specialist
- Medical Writer
Skills Required for Success
To perform effectively as a Clinical Research Coordinator, candidates should possess:
Communication Skills
Since CRCs interact with patients, investigators, and sponsors, excellent communication is essential.
Attention to Detail
Clinical research documentation requires high levels of accuracy and precision.
Organizational Skills
Managing multiple study activities simultaneously requires strong planning abilities.
Ethical Mindset
Patient safety and data integrity should always remain top priorities.
Computer Skills
Knowledge of:
- MS Excel
- MS Word
- Clinical databases
- Documentation systems
can be beneficial.
Importance of Good Clinical Practice (GCP)
Good Clinical Practice (GCP) is an internationally recognized quality standard for conducting clinical trials.
GCP ensures:
- Participant safety
- Data integrity
- Ethical conduct
- Regulatory compliance
Candidates possessing GCP certification often gain a competitive advantage during recruitment.
If you have completed any online GCP training course, be sure to mention it prominently in your resume.
Work Location Details
The available positions are located in:
Delhi
Delhi is one of India’s largest healthcare and pharmaceutical hubs, offering numerous opportunities in clinical research, healthcare services, and pharmaceutical development.
Faridabad
Faridabad is emerging as an important center for healthcare institutions and clinical trial activities within the National Capital Region (NCR).
Candidates should be comfortable commuting and traveling locally when required for study-related activities.
Tips to Improve Your Chances of Selection
Build a Professional Resume
Your resume should clearly highlight:
- Educational qualifications
- Clinical research internships
- Academic projects
- GCP certifications
- Research experience
Learn Clinical Research Basics
Understanding the following concepts can significantly improve interview performance:
- Clinical Trial Phases
- GCP Guidelines
- Informed Consent
- Adverse Event Reporting
- Ethics Committee Functions
Prepare for Interviews
Common interview questions may include:
- What is clinical research?
- What is GCP?
- What is informed consent?
- What are adverse events?
- Why do you want to become a CRC?
How to Apply
Interested candidates can submit their applications using the details below.
Email Application
📧 Email: shivensisresearch@gmail.com
Suggested Subject Line
- Application for CRC Position – Fresher – B.Pharm – Delhi
- Application for Clinical Research Coordinator – M.Sc Biotechnology – Faridabad
- CRC Application – Pharm.D Graduate – NCR Region
Important Resume Checklist
Before sending your application, ensure your resume includes:
✅ Educational Qualifications
✅ Internship Experience
✅ Clinical Research Training
✅ GCP Certification
✅ Communication Skills
✅ Contact Information
✅ Professional Email Address
Final Thoughts
The Clinical Research Coordinator position at Shivensis Research offers an excellent opportunity for fresh graduates to begin a rewarding career in the pharmaceutical and clinical research industry. With direct exposure to clinical trials, patient interactions, regulatory processes, and healthcare innovation, this role provides a strong foundation for future growth.
If you are passionate about healthcare, research, patient safety, and scientific advancement, this CRC opportunity in Delhi and Faridabad could be the perfect first step toward a successful career in clinical research.
Since only two openings are currently available, interested candidates should apply as early as possible and ensure their resumes highlight relevant academic achievements, internships, and certifications.
Start your journey into the world of clinical research today and take the first step toward becoming a future Clinical Research Associate, Project Manager, or Clinical Operations Leader.
Related Pharma, Clinical Research & Healthcare Career Opportunities
Entry-Level Pharma Sales Careers
Global Regulatory Affairs Specialist Jobs
Clinical Research Careers in Ahmedabad
Pharmaceutical Product Management Jobs
Healthcare Business Development Careers
Patent and Intellectual Property Careers
Medical Affairs Careers in Pharma Industry
Pharmaceutical Quality Control Careers
