This opportunity is suitable for professionals who have experience managing clinical trial activities, coordinating with investigators and sponsors, maintaining regulatory documentation, and ensuring compliance with clinical research standards.
Immediate joiners with relevant CRC experience are preferred.
Job Overview
| Particulars | Details |
|---|---|
| Position | Clinical Research Coordinator (CRC) |
| Company | Dhanvanthari Clinical Research |
| Location | Bangalore, Karnataka |
| Job Type | Full-Time |
| Experience | 1 - 8 years |
| Category / Department | CDM |
| Application Mode |
π’ About Dhanvanthari Clinical Research
Dhanvanthari Clinical Research is a Clinical Research Organization (CRO) and Site Management Organization (SMO) focused on supporting clinical trials with quality-driven research solutions.
The organization works with sponsors, CRO partners, investigators, trial sites, and patients to enable efficient clinical development programs.
Its services include clinical trial management, site support, regulatory assistance, patient recruitment, monitoring support, pharmacovigilance, data management, and other clinical research solutions.
π Job Description
Dhanvanthari Clinical Research Hiring | Clinical Research Coordinator (CRC) | Clinical Research Jobs
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π’ Company: Dhanvanthari Clinical Research
πΌ Position: Clinical Research Coordinator (CRC)
π Location: Bangalore, Karnataka
π§ͺ Department: Clinical Research
β³ Experience: Experienced Candidates
π¬ Study Experience: Ophthalmology / Dermatology Clinical Studies
π Job Type: Full-Time
π© Application Mode: Email Application
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Required Qualifications
Candidates should have:
π Bachelorβs or Masterβs degree in:
β’ Life Sciences
β’ Pharmacy
β’ Nursing
β’ Biotechnology
β’ Related healthcare disciplines
Experience Required:
β’ Previous experience as Clinical Research Coordinator (CRC).
β’ Experience in Ophthalmology or Dermatology clinical research is mandatory.
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Why Join Dhanvanthari Clinical Research?
β Opportunity to work on specialized clinical studies.
β Exposure to regulated clinical research projects.
β Career growth opportunities in CRO and clinical operations.
β Experience working with investigators, sponsors, and research teams.
β Professional learning environment.
β Immediate joining opportunities for eligible candidates.
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How to Apply?
Interested candidates can share their updated resume at:
π§ Email: dreshwari@dhanvantharicr.com
π― Key Responsibilities
- β Selected Clinical Research Coordinator will be responsible for:
- β Coordinate and manage Ophthalmology or Dermatology clinical studies.
- β Support patient screening, recruitment, enrollment, and follow-up activities.
- β Ensure compliance with ICH-GCP guidelines, SOPs, and regulatory requirements.
- β Maintain accurate source documents, study files, and essential clinical trial records.
- β Coordinate with Principal Investigators, sponsors, CRO teams, and ethics committees.
- β Prepare and maintain trial-related documentation.
- β Track study timelines and ensure completion of assigned activities.
- β Support monitoring visits, audits, and regulatory inspections.
- β Report adverse events and study-related updates as per protocol requirements.
- β Ensure quality and accuracy throughout clinical trial execution.
π‘ Required Qualifications & Skills
Frequently Asked Questions
Q1. What is the job role available at Dhanvanthari Clinical Research?
The company is hiring for the position of Clinical Research Coordinator (CRC).
Q2. What experience is required for this CRC position?
Candidates should have prior Clinical Research Coordinator experience, preferably in Ophthalmology or Dermatology studies.
Q3. What qualifications are required?
Applicants should have a Bachelorβs or Masterβs degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or related fields.
Q4. Where is this job located?
The position is based in Bangalore, Karnataka.
Q5. How can candidates apply?
Eligible candidates can send their updated resume to dreshwari@dhanvantharicr.com.
Q6. Is immediate joining preferred?
Yes, immediate joiners with relevant experience are preferred.