Latest pharma jobs for freshers and experienced candidates in clinical research coordinator role apply online now with eligibility details and updates
Introduction
The healthcare research sector in India is rapidly expanding, creating strong demand for skilled professionals in clinical operations. The Clinical Research Coordinator Jobs in HRAPL offer an excellent opportunity for experienced candidates to work at the forefront of clinical trials. This role is ideal for individuals who have hands-on experience in patient coordination, site management, and regulatory compliance. If you are aiming to grow in clinical research, this position provides a stable and rewarding career path.
Job Overview
| Job Title | Clinical Research Coordinator (CRC) |
|---|---|
| Company Name | HRAPL |
| Location | Rishikesh, Uttarakhand |
| Employment Type | Full-Time |
| Department | Clinical Research |
| Experience Required | 3–4 Years |
| Education | Life Sciences / Pharmacy / Related Field |
| Salary | As per company norms |
Company Overview
HRAPL is an emerging organization in the clinical research domain, focusing on delivering high-quality research support and site management services. The company works closely with investigators, sponsors, and healthcare institutions to ensure smooth execution of clinical trials while maintaining strict compliance with regulatory standards.
Being part of such an organization allows professionals to gain practical exposure to real-world clinical research environments and regulated trial processes.
Job Location & Employment Type
- Location: Rishikesh, Uttarakhand
- Employment Type: Full-Time
- Work Mode: On-site (Clinical Trial Site-Based Role)
This position requires candidates to work directly at the clinical trial site, managing day-to-day research activities.
Open Positions / Department Details
- Clinical Operations
- Site Management
- Patient Coordination
The role primarily revolves around managing clinical trial activities at the site level and ensuring smooth execution of protocols.
Key Roles & Responsibilities
As a Clinical Research Coordinator, your responsibilities will include:
- Coordinating and managing clinical trial site activities efficiently
- Handling patient recruitment, scheduling visits, and follow-ups
- Ensuring proper execution of Informed Consent Form (ICF) procedures
- Maintaining accurate source documents and clinical records
- Ensuring adherence to study protocols and ICH-GCP guidelines
- Assisting in monitoring visits, audits, and regulatory inspections
- Collaborating with investigators, sponsors, and CRO teams
- Tracking patient safety and reporting adverse events as per protocol
- Managing trial documentation and ensuring data accuracy
- Supporting overall site compliance and quality standards
Eligibility Criteria
Education
Candidates must have a degree in:
- Life Sciences
- Pharmacy
- Or any related healthcare discipline
Experience
- Minimum 3 to 4 years of experience as a Clinical Research Coordinator (CRC)
- Experience in clinical trial site handling is essential
Skills Required
- Strong knowledge of ICH-GCP guidelines
- Understanding of clinical trial processes and regulations
- Experience in patient coordination and documentation
- Good communication and organizational skills
- Attention to detail and compliance-focused approach
- Ability to manage multiple tasks in a clinical setting
Salary & Benefits
- Salary: As per company norms
- Exposure to structured clinical research processes
- Opportunity to work in regulated trial environments
- Career growth in clinical operations and site management
- Industry-standard benefits and learning opportunities
Selection Process
The hiring process may include:
- Resume screening
- Initial HR discussion
- Technical interview (clinical research knowledge)
- Final selection and offer
How to Apply
Interested candidates can apply via email with their updated CV:
📧 contact@hrapl.in
Subject Line: Name_CRC_Rishikesh
Make sure to mention relevant clinical research experience clearly in your resume.
Important Dates
- Last Date to Apply: Not specified (Apply early to avoid missing the opportunity)
Why Apply for This Job?
The Clinical Research Coordinator Jobs in HRAPL provide a strong platform for career advancement in clinical research. Here’s why this opportunity stands out:
- Work directly on clinical trial sites with real patient interaction
- Gain hands-on experience in regulatory-compliant environments
- Improve expertise in clinical documentation and patient handling
- Opportunity to collaborate with experienced investigators and research teams
- Build a long-term career in clinical operations and site management
This role is especially beneficial for professionals aiming to transition into advanced roles such as Clinical Research Associate (CRA) or Clinical Project Manager.
FAQs
1. What is the required experience for this CRC job?
Candidates must have 3–4 years of experience as a Clinical Research Coordinator.
2. What qualifications are required?
A degree in Life Sciences, Pharmacy, or a related field is required.
3. Is this a remote job?
No, this is an on-site role based in Rishikesh.
4. What skills are important for this position?
Knowledge of ICH-GCP, patient handling, and clinical documentation is essential.
5. How can I apply for this job?
You can apply by sending your CV to the provided email with the correct subject line.
Conclusion
The Clinical Research Coordinator Jobs in HRAPL offer a valuable opportunity for experienced professionals to strengthen their careers in clinical research. With hands-on site experience, exposure to regulatory processes, and growth potential, this role is ideal for candidates seeking stability and advancement in the healthcare research field. Apply early to secure your chance in this competitive opportunity.
Disclaimer
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