Leading Clinical Trials Professional
2 days ago
About Us:
We are a fast-growing Clinical Trials Organization dedicated to providing high-quality, ethical, and efficient clinical trial services. We are committed to excellence in research and uphold the highest standards of regulatory compliance and data integrity.
Job Summary:
We are seeking an experienced Senior Clinical Research Coordinator (CRC) to join our dynamic team. The ideal candidate will have a strong understanding of clinical trial processes, GCP guidelines, and sponsor protocols, with at least 1.5 years of hands-on experience coordinating clinical trials.
Key Responsibilities:
- Coordinate and manage day-to-day clinical trial activities at the site.
- Ensure compliance with study protocols, ICH-GCP, and applicable regulatory requirements.
- Manage subject recruitment, informed consent process, screening, enrollment, and follow-up visits.
- Collect and enter accurate source data and case report forms (CRFs) in a timely manner.
- Act as a primary liaison between the site, sponsors, and monitors.
- Prepare for and support monitoring visits, audits, and regulatory inspections.
- Maintain and organize study documentation (ISF, logs, accountability records, etc.).
Qualifications & Skills:
- Bachelor's degree in life sciences, pharmacy, nursing, or a related field.
- Minimum of 1.5 years of experience coordinating clinical trials.
- Strong knowledge of ICH-GCP, Indian regulatory requirements, and ethical guidelines.
- Excellent organizational and communication skills.
- Proficient in Microsoft Office and electronic data capture (EDC) systems.
- Ability to work independently and handle multiple tasks efficiently.
What We Offer:
- A collaborative and supportive work environment.
- Opportunities for professional growth and training.
- Competitive salary and performance-based incentives.
- Exposure to a diverse portfolio of clinical studies.
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