HRAPL is hiring for a Clinical Research Coordinator job in Mumbai for candidates with experience in clinical trial site operations. This opportunity is suitable for graduates in Life Sciences, Biotechnology, Pharmacy, or related disciplines who have 3–4 years of relevant clinical research experience.
The Clinical Research Coordinator will be responsible for managing day-to-day clinical trial site activities, coordinating patient workflows, maintaining accurate study documentation, and supporting investigators, Clinical Research Associates (CRAs), and other site personnel.
Candidates should have practical knowledge of ICH-GCP, clinical study protocols, informed consent processes, essential documentation, and applicable regulatory requirements. Immediate joiners will be preferred.
Job Overview
| Particular | Details |
|---|---|
| Company | HRAPL |
| Position | Clinical Research Coordinator (CRC) |
| Department | Clinical Research / Clinical Operations |
| Qualification | Graduate in Life Sciences, Biotechnology, Pharmacy, or related fields |
| Experience | 3–4 years |
| Location | Mumbai, Maharashtra |
| Openings | 1 |
| Joining Preference | Immediate joiners preferred |
| Employment Type | Full-time |
| Application Mode |
Key Responsibilities
As a Clinical Research Coordinator at HRAPL, the selected candidate will support efficient and compliant execution of clinical studies at the site level. Key responsibilities are expected to include:
- Coordinate day-to-day clinical trial site operations and study activities.
- Manage patient-related workflows according to study protocols.
- Support patient coordination and clinical study visit activities.
- Handle the Informed Consent Form (ICF) process and related documentation.
- Maintain accurate, complete, and timely essential clinical trial documentation.
- Coordinate effectively with investigators, CRAs, site personnel, and other stakeholders.
- Ensure study activities are conducted according to approved clinical trial protocols.
- Support compliance with ICH-GCP and applicable regulatory requirements.
- Maintain high standards of documentation accuracy and protocol compliance.
- Help ensure smooth communication and coordination across clinical study activities.
Eligibility and Qualifications
Candidates interested in the HRAPL Clinical Research Coordinator vacancy in Mumbai should meet the following requirements:
Educational Qualification: Graduate degree in Life Sciences, Biotechnology, Pharmacy, or a related field.
Experience: Applicants should have 3–4 years of experience in clinical trial site operations.
Candidates should also have:
- Experience in patient coordination.
- Knowledge of ICF handling and informed consent processes.
- Experience maintaining essential clinical trial documentation.
- Ability to coordinate with investigators, CRAs, and site teams.
- Working knowledge of ICH-GCP guidelines.
- Understanding of clinical study protocols.
- Knowledge of relevant clinical research regulatory requirements.
- Strong attention to detail and coordination skills.
This is an experienced-hire position; the vacancy specifically requires 3–4 years of clinical trial site operations experience.
Key Skills
Clinical Research Coordinator (CRC), Clinical Research, Clinical Trials, Clinical Operations, Site Management, Patient Coordination, Informed Consent Form, ICF Handling, Essential Documents, ICH-GCP, Clinical Trial Documentation, Study Protocols, Investigator Coordination, CRA Coordination, Regulatory Compliance, Site Operations.
Why Consider This Opportunity?
The Clinical Research Coordinator job at HRAPL offers experienced clinical research professionals an opportunity to work directly with site-level clinical trial operations in Mumbai.
The position provides exposure to patient coordination, investigator and CRA communication, essential study documentation, protocol compliance, and ICH-GCP-based clinical research activities. It may be particularly relevant for professionals seeking to strengthen their experience in clinical trial site management and clinical operations.
Note: Specific employee benefits, incentives, insurance, or other compensation benefits were not mentioned in the original recruitment information. Candidates should confirm these directly with HR during the selection process.
Estimated Salary
HRAPL has not disclosed the salary for this position in the supplied job announcement.
For structured-data purposes, a reasonable estimated market range for a Clinical Research Coordinator with 3–4 years of relevant experience in Mumbai may be approximately ₹4,00,000–₹7,00,000 per year.
This is an estimated range only and is not an employer-disclosed salary. Actual compensation may vary depending on experience, skills, current CTC, interview performance, and HRAPL’s compensation structure.
How to Apply for HRAPL CRC Job
Eligible candidates can apply by emailing their updated resume to:
Email: contact@hrapl.in
