HRAPL is hiring for a Clinical Research Coordinator (CRC) position in Wardha, Maharashtra. This opportunity is suitable for graduates in Life Sciences, Biotechnology, Pharmacy, and related disciplines who have 2–3 years of experience in clinical trial site operations.
The Clinical Research Coordinator will be responsible for supporting day-to-day clinical research activities, coordinating patient workflows, maintaining essential study documentation, and working closely with investigators, Clinical Research Associates (CRAs), and other site team members.
Candidates with hands-on knowledge of ICH-GCP, informed consent (ICF) procedures, clinical trial protocols, patient coordination, and regulatory documentation are encouraged to apply. Immediate joiners will be preferred.
HRAPL Clinical Research Coordinator Job Overview
| Particulars | Details |
|---|---|
| Company | HRAPL |
| Position | Clinical Research Coordinator (CRC) |
| Openings | 1 |
| Qualification | Graduate in Life Sciences, Biotechnology, Pharmacy, or related fields |
| Experience | 2–3 Years |
| Location | Wardha, Maharashtra |
| Industry | Clinical Research / Clinical Trials |
| Employment Type | Full-Time |
| Joining Preference | Immediate Joiners Preferred |
Who Can Apply?
Candidates with a graduate degree in Life Sciences, Biotechnology, Pharmacy, or a related discipline can apply for the HRAPL Clinical Research Coordinator job.
Applicants should have 2–3 years of relevant experience in clinical trial site operations.
Eligible degrees may include: B.Pharm, B.Sc Life Sciences, B.Sc Biotechnology, and other relevant graduate-level Life Sciences or clinical research-related qualifications, subject to HRAPL’s final eligibility assessment.
Key Responsibilities
As a Clinical Research Coordinator at HRAPL, the selected candidate will support the effective execution of clinical studies at the site. Key responsibilities are expected to include:
- Coordinate daily clinical trial site activities and patient workflows.
- Support patient screening, scheduling, follow-ups, and study-related coordination.
- Handle informed consent documentation and ensure proper ICF procedures are followed.
- Maintain accurate and complete essential clinical trial documentation.
- Coordinate effectively with Principal Investigators, CRAs, patients, and site personnel.
- Follow approved study protocols and site procedures.
- Support compliance with ICH-GCP and applicable regulatory requirements.
- Help maintain study documentation in a timely and inspection-ready manner.
- Ensure accurate coordination of trial-related activities throughout the study lifecycle.
Eligibility & Qualifications
Candidates applying for the HRAPL Clinical Research Coordinator vacancy in Wardha should meet the following requirements:
Educational Qualification: Graduate in Life Sciences, Biotechnology, Pharmacy, or related fields.
Experience: 2–3 years of experience in clinical trial site operations.
Candidates should also have practical knowledge or experience in:
- Patient coordination
- Informed Consent Form (ICF) handling
- Essential clinical trial documentation
- Clinical trial site operations
- ICH-GCP guidelines
- Study protocols
- Regulatory requirements
- Investigator and CRA coordination
Strong communication, organizational ability, attention to detail, and protocol compliance will be important for this Clinical Research Coordinator role.
Skills Required
The HRAPL CRC position requires a combination of clinical research knowledge and strong site coordination capabilities. Relevant skills include clinical trial coordination, patient management, ICF handling, clinical documentation, ICH-GCP compliance, protocol adherence, investigator coordination, CRA coordination, and regulatory compliance.
Candidates should be comfortable managing multiple site activities while maintaining accurate documentation and ensuring that trial activities follow the approved protocol.
Why Consider This Opportunity?
This Clinical Research Coordinator position provides experienced clinical research professionals an opportunity to strengthen their exposure to site-level clinical trial operations, patient coordination, investigator interaction, clinical documentation, and regulatory compliance.
The role may be particularly relevant for candidates seeking to build further experience in clinical research site operations and potentially progress toward senior CRC, Clinical Trial Assistant, Site Management, or CRA-related career paths.
Note: HRAPL’s original recruitment information does not specify salary, incentives, insurance, or other employee benefits. Candidates should confirm compensation and benefits directly with the employer during the recruitment process.
Salary
HRAPL has not disclosed the official salary for this Clinical Research Coordinator vacancy.
For structured job-data purposes, an indicative market estimate of approximately ₹3,00,000–₹5,00,000 per year may be considered for a CRC with 2–3 years of experience in Maharashtra. This is not an HRAPL-confirmed salary and actual compensation may vary based on experience, skills, current CTC, and company policy.
How to Apply for HRAPL CRC Job
Interested and eligible candidates can send their updated resume to:
Email: contact@hrapl.in