Clinical Research Coordinator: Are you looking to start or grow your career in clinical research, healthcare studies, or clinical trial coordination? A new opportunity is now open for the position of Clinical Research Coordinator (CRC) in Agra, offering a flexible, part-time and project-based role for candidates interested in gaining real-world experience in clinical research.
This position is ideal for freshers, trainees, and early-career professionals in life sciences, pharmacy, and nursing backgrounds who want to build hands-on expertise in clinical trials, patient data management, and research coordination while working on impactful healthcare projects.
With the growing demand for skilled professionals in clinical research and trial management, this opportunity provides a strong foundation to enter and grow within the pharmaceutical, biotechnology, and healthcare research industries.
Job Location
Agra, Uttar Pradesh, India
This is primarily a field-based role, requiring candidates to visit clinical sites and coordinate with healthcare professionals and research teams.
Job Type
- Part-Time
- Project-Based
- Flexible Working Opportunity
This role is designed for individuals who prefer flexible work schedules while gaining valuable experience in clinical research operations.
Detailed Job Overview of Clinical Research Coordinato
The Clinical Research Coordinator (CRC) will be responsible for supporting ongoing clinical research projects by ensuring smooth coordination between patients, investigators, and research teams. The role involves a combination of fieldwork, data entry, documentation management, and patient tracking.
As a CRC, you will play a crucial role in maintaining the accuracy, integrity, and compliance of clinical trial data, which directly contributes to the success of research studies and advancements in healthcare.
This position is particularly suitable for candidates who are detail-oriented, organized, and interested in working at the intersection of healthcare, data, and clinical science.
Key Responsibilities
- Conduct site visits to hospitals, clinics, or research centers as required
- Assist in patient enrollment tracking and follow-ups
- Perform accurate data entry into Case Report Forms (CRF) and electronic CRFs (eCRF)
- Maintain and organize clinical trial documentation and study records
- Support investigators in resolving data queries and discrepancies
- Ensure proper documentation in compliance with clinical protocols and regulatory guidelines
- Coordinate with research teams to ensure smooth execution of clinical studies
- Monitor study progress and assist in maintaining timelines
- Ensure confidentiality and secure handling of patient data
Eligibility Criteria
- Graduate degree in:
- Life Sciences
- Pharmacy
- Nursing
- Or related healthcare/biomedical fields
- Basic understanding of:
- Clinical research processes
- Clinical trial documentation
- ICH-GCP guidelines (preferred but not mandatory)
- Good communication and coordination skills
- Strong attention to detail and organizational abilities
- Willingness to travel locally for site visits
Preferred Skills
- Knowledge of clinical trial phases and research workflows
- Familiarity with CRF/eCRF data entry systems
- Basic computer skills (MS Excel, Word, documentation tools)
- Ability to manage multiple tasks and meet deadlines
- Problem-solving mindset and proactive approach
Compensation Structure
- Performance-based payment model
- Payment on a per-patient or per-task basis
- Opportunity to increase earnings based on performance and involvement in multiple projects
This model allows candidates to earn while learning and grow their experience simultaneously.
Why You Should Apply
- Flexible, project-based work structure
- Hands-on exposure to real clinical research projects
- Opportunity to work directly with healthcare professionals and investigators
- Build practical skills in clinical trials, data management, and patient coordination
- Strong career pathway into roles like:
- Clinical Research Associate (CRA)
- Clinical Trial Coordinator
- Clinical Data Manager
- Pharmacovigilance Associate
- Gain industry-relevant experience that is highly valued in pharma and biotech companies
Career Growth Opportunities
Working as a Clinical Research Coordinator (CRC) is one of the best entry points into the clinical research industry. With experience, you can advance into higher roles such as:
- Clinical Research Associate (CRA)
- Senior CRC or Site Coordinator
- Clinical Data Manager
- Regulatory Affairs Specialist
- Medical Research Analyst
This role helps you develop a strong understanding of clinical trial operations, regulatory compliance, and patient data management, which are essential for long-term success in the healthcare research domain.
How to Apply
Interested candidates can share their updated CV/resume at:
Make sure your CV highlights:
- Educational background
- Any internships or experience in clinical research or healthcare
- Relevant technical or documentation skills
Final Thoughts
The demand for skilled professionals in clinical research and healthcare data management is rapidly increasing. This part-time Clinical Research Coordinator job in Agra offers a great opportunity to gain practical exposure, flexible working experience, and industry-relevant skills.
Whether you are a fresher or someone looking to transition into the clinical research field, this role can serve as a strong stepping stone toward a successful and rewarding career.
FAQs
Q1. Is this job suitable for freshers?
Yes, freshers and trainees with basic knowledge of clinical research can apply.
Q2. Is this a full-time job?
No, this is a part-time, project-based role with flexible working hours.
Q3. Do I need prior experience in clinical research?
Not mandatory, but basic knowledge of clinical research and ICH-GCP is preferred.
Q4. What kind of work will I do?
You will assist in patient tracking, data entry (CRF/eCRF), documentation, and site coordination.
