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 |
🏢 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.
📝 Job Description
Dhanvanthari Clinical Research Hiring | Clinical Research Coordinator (CRC) | Clinical Research Jobs
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🏢 Company: Dhanvanthari Clinical Research
💼 Position: Clinical Research Coordinator (CRC)
📍 Location: Bangalore, Karnataka
🧪 Department: Clinical Research
⏳ Experience: Experienced Candidates
🔬 Study Experience: Ophthalmology / Dermatology Clinical Studies
📌 Job Type: Full-Time
📩 Application Mode: Email Application
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Required Qualifications
Candidates should have:
🎓 Bachelor’s or Master’s degree in:
• Life Sciences
• Pharmacy
• Nursing
• Biotechnology
• Related healthcare disciplines
Experience Required:
• Previous experience as Clinical Research Coordinator (CRC).
• Experience in Ophthalmology or Dermatology clinical research is mandatory.
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Why Join Dhanvanthari Clinical Research?
✔ Opportunity to work on specialized clinical studies.
✔ Exposure to regulated clinical research projects.
✔ Career growth opportunities in CRO and clinical operations.
✔ Experience working with investigators, sponsors, and research teams.
✔ Professional learning environment.
✔ Immediate joining opportunities for eligible candidates.
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How to Apply?
Interested candidates can share their updated resume at:
📧 Email: dreshwari@dhanvantharicr.com
🎯 Key Responsibilities
- ✓ Selected Clinical Research Coordinator will be responsible for:
- ✓ Coordinate and manage Ophthalmology or Dermatology clinical studies.
- ✓ Support patient screening, recruitment, enrollment, and follow-up activities.
- ✓ Ensure compliance with ICH-GCP guidelines, SOPs, and regulatory requirements.
- ✓ Maintain accurate source documents, study files, and essential clinical trial records.
- ✓ Coordinate with Principal Investigators, sponsors, CRO teams, and ethics committees.
- ✓ Prepare and maintain trial-related documentation.
- ✓ Track study timelines and ensure completion of assigned activities.
- ✓ Support monitoring visits, audits, and regulatory inspections.
- ✓ Report adverse events and study-related updates as per protocol requirements.
- ✓ Ensure quality and accuracy throughout clinical trial execution.
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Clinical Research Coordinator (CRC) role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
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 Bachelor’s or Master’s 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.
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