About Us: Kairos R and D Solutions Pvt. Ltd. is a fast-growing Clinical Trials Organization based in Hyderabad, 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 Description: We are seeking a dedicated and experienced Senior Clinical Research Coordinator (CRC) to join our dynamic team in Hyderabad. The ideal candidate will have a strong understanding of clinical trial processes, GCP guidelines, and sponsor protocols, with at least one year 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.). Train and mentor junior coordinators as needed. 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. Show more Show less

About Us: Kairos R and D Solutions Pvt. Ltd. is a fast-growing Clinical Trials Organization based in Hyderabad, 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 Description: We are seeking a dedicated and experienced Clinical Research Coordinator (CRC) to join our dynamic team in Hyderabad. The ideal candidate will have a strong understanding of clinical trial processes, GCP guidelines, and sponsor protocols, with at least one year 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.). Train and mentor junior coordinators as needed. Qualifications & Skills: Bachelor’s degree in life sciences, pharmacy, nursing, or a related field. Minimum of 1 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.