Harrison’s Tech Consultants (HTC) is hiring a Clinical Research Coordinator for its clinical operations in Navi Mumbai. This is a full-time, on-site opportunity involving patient coordination, clinical trial documentation, regulatory compliance and site-management activities.
The position may suit candidates with qualifications in life sciences, pharmacy, nursing or clinical research. Previous CRC or clinical trial site-management experience is preferred, but the employer has not specified a mandatory number of years.
Quick answer: Harrison’s Tech Consultants is hiring a Clinical Research Coordinator in Navi Mumbai. Candidates with a bachelor’s degree in life sciences, pharmacy, nursing or a related field and knowledge of GCP, patient coordination and clinical trial documentation can apply.
Job Overview
| Particular | Details |
|---|---|
| Company | Harrison’s Tech Consultants (HTC) |
| Role | Clinical Research Coordinator |
| Location | Navi Mumbai, Maharashtra |
| Work mode | On-site |
| Job type | Full-time |
| Experience | Prior CRC or site-management experience preferred |
| Qualification | Bachelor’s degree in Life Sciences, Pharmacy, Nursing or related field |
| Estimated salary | ₹3–6 LPA |
| Posted date | August 13, 2026 |
| Last date | Not specified |
| Application mode | LinkedIn Easy Apply |
About Harrison’s Tech Consultants
Harrison’s Tech Consultants is a hospitals and healthcare solutions company operating in Mumbai and Delhi. Its work covers regulatory consulting for drugs and medical devices, project management and clinical trial site-management services.
The organization works with patients, investigators, sponsors and contract research organizations to support compliant and quality-focused clinical trial execution.
Responsibilities
The selected Clinical Research Coordinator will be expected to:
- Support the planning, execution and monitoring of clinical trials.
- Implement study protocols at the assigned clinical trial site.
- Coordinate patient identification, recruitment and screening.
- Schedule patient visits according to study requirements.
- Support the informed-consent process.
- Maintain accurate source documents and case report forms.
- Enter or review study information in applicable data systems.
- Manage investigational supplies, study materials and biological samples.
- Communicate with investigators, site employees, sponsors and CRO teams.
- Report adverse events and serious adverse events promptly.
- Document and report protocol deviations.
- Assist with ethics and regulatory submissions.
- Prepare study records for monitoring visits and audits.
- Support site-level quality assurance activities.
- Ensure compliance with GCP, ICH guidelines and local regulations.
- Protect patient safety, privacy and study-data integrity.
Qualifications: Who Can Apply?
Candidates should have:
- A bachelor’s degree in life sciences, pharmacy, nursing or a related discipline.
- Knowledge of clinical research operations and trial-site activities.
- Understanding of Good Clinical Practice and ICH guidelines.
- Familiarity with ethical and regulatory requirements for clinical trials.
- Knowledge of source documentation and case report forms.
- Basic proficiency in Microsoft Office and digital clinical research tools.
- Ability to work on-site in a hospital or clinical environment in Navi Mumbai.
- Flexibility to support study visits according to the required schedule.
Advanced qualifications or certifications in clinical research will be an advantage.
Previous experience as a Clinical Research Coordinator or in clinical trial site management is preferred. The listing does not state a mandatory experience duration, but it should not be presented as a confirmed fresher opening.
Qualification in one line: Bachelor’s degree in Life Sciences, Pharmacy, Nursing or a related field; advanced qualifications or certifications in Clinical Research are advantageous.
Skills Required
Technical Skills
- Source-document maintenance
- Case report form completion
- Electronic Data Capture basics
- Microsoft Office
- Clinical trial documentation
- Adverse event reporting
- Study-supply and sample management
- Basic clinical trial management systems
Domain Skills
- Clinical research operations
- Protocol implementation
- Patient recruitment and screening
- Informed consent
- Visit coordination
- GCP and ICH guidelines
- Regulatory and ethics compliance
- Protocol-deviation management
- Audit preparation
- Patient-safety requirements
Soft Skills
- Communication
- Patient coordination
- Time management
- Attention to detail
- Multitasking
- Team collaboration
- Organizational ability
- Professional documentation
Estimated Salary
The employer has not disclosed the compensation in the job listing.
Estimated salary range: ₹3–6 LPA.
This is an editorial estimate based on the position, location and preferred experience. The actual salary may depend on the candidate’s qualifications, clinical research experience and interview performance.
Is This Position Open to Freshers?
The employer has not explicitly described this as a fresher position. Previous experience as a Clinical Research Coordinator or in clinical trial site management is listed as preferred, not clearly mandatory.
Candidates with relevant clinical research training, internships, hospital exposure or site-level project experience may still consider applying if they satisfy the remaining requirements. Selection will remain at the employer’s discretion.
Benefits
Benefits were not clearly specified in the job description.
How to Apply
