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Clindus Research Solutions, a leading Site Management Organization (SMO), is hiring a Clinical Research Coordinator (CRC) in Hubli, Karnataka. This role is ideal for candidates passionate about clinical research, patient recruitment, and regulatory compliance. With the growing demand for skilled clinical research professionals in India, this position offers an excellent opportunity to kickstart or advance your career in the healthcare and research sector.
Key Responsibilities
As a Clinical Research Coordinator, you will:
- Obtain informed consent from study participants.
- Conduct protocol reviews and ensure adherence to clinical trial protocols.
- Oversee patient recruitment and screening processes.
- Maintain accurate clinical trial records and source documentation.
- Ensure compliance with regulatory and ethical guidelines.
- Collaborate with investigators, site staff, and sponsors.
- Manage day-to-day operations of clinical trials at the site.
Required Qualifications
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
- 6 months to 1 year of hands-on clinical research experience.
- Strong knowledge of clinical trial procedures and GCP guidelines.
- Experience with informed consent and protocol reviews.
- Proficiency in Microsoft Office; CTMS knowledge is an added advantage.
- Excellent organizational, communication, and time-management skills.
Benefits of Working with Clindus Research Solutions
- Hands-on exposure to global clinical trials.
- Career growth opportunities in a fast-growing SMO.
- Collaborative work environment with industry experts.
- Competitive salary package (INR 3,00,000 – 4,50,000 per year).
How to Apply
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