Clindus is hiring Clinical Research Coordinators (CRC) in Hubli to strengthen its growing clinical trials team. This is an excellent opportunity for both fresh graduates in life sciences, pharmacy, or clinical research as well as experienced CRCs with hands-on site management exposure.
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If you’re based in the Hubli-Dharwad district and passionate about advancing ethical, compliant, and impactful clinical research, this role is for you.
Open Positions
- Experienced CRC – Minimum 6 months to 1 year of clinical trial coordination, documentation, and site management experience.
- Trainee CRC – Freshers/early-career candidates with a B.Sc, M.Sc, B.Pharm, or M.Pharm background. Full training will be provided.
Location: Hubli, Karnataka
Preference: Candidates residing in or around Hubli-Dharwad
Key Responsibilities
- Support clinical trial activities including documentation and regulatory compliance
- Assist in subject screening, recruitment, and informed consent process
- Coordinate with investigators, sponsors, and ethics committees
- Maintain accurate source documents and ensure protocol adherence
- Facilitate monitoring visits and maintain audit readiness
Preferred Qualifications
- B.Sc / M.Sc in Life Sciences
- B.Pharm / M.Pharm or equivalent
- Strong interest in clinical research and regulatory guidelines
- For experienced roles: minimum 6 months of CRC experience
Benefits of Joining
- Hands-on experience in clinical trials in Karnataka
- Structured training program for trainee CRCs
- Opportunity to work on industry-standard protocols
- Career growth in clinical research coordination
How to Apply
Interested candidates can send their updated CV to:
📧 hr@clindus.in
Subject line: CRC Application – Hubli, Karnataka
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