CRC

Company Description Dhanvantari Clinical Research Solutions is a full-service Clinical Research Organization (CRO) and Site Management Organization (SMO) focused on accelerating the success of clinical trials. The company collaborates closely with sponsors, CRO partners, trial sites, investigators, and patients to support the entire clinical development lifecycle. As a CRO, it provides end-to-end services such as protocol development, trial management, regulatory submissions, data management, pharmacovigilance, medical writing, and biostatistics, ensuring accuracy and regulatory compliance. As an SMO, it offers site identification, investigator support, ethics submissions, patient recruitment and retention, and site monitoring assistance to reduce site burden and improve operational efficiency. This integrated approach enables faster, higher-quality clinical trials and creates opportunities for professionals to contribute meaningfully to advancing clinical research.
Role Description The Clinical Research Coordinator (CRC) is a full-time, on-site role based in Mysuru, responsible for coordinating and supporting clinical trial activities at assigned study sites. The CRC will manage day-to-day trial operations, including screening and enrolling participants, scheduling visits, and ensuring that all study procedures are conducted according to the protocol, Good Clinical Practice (GCP), and applicable regulations. The role includes maintaining accurate and timely source documentation, case report forms, and regulatory files, as well as assisting with ethics committee submissions and ongoing communications. The CRC will collaborate closely with investigators, study nurses, monitors, and other site staff to facilitate patient recruitment, retention, and compliance with study requirements. The position also involves handling query resolution, preparing for monitoring and audit visits, and contributing to continuous improvement in site processes and patient experience.
Qualifications

• Strong clinical research coordination skills, including protocol adherence, visit scheduling, and management of source documents and case report forms.
• Knowledge of Good Clinical Practice (GCP), ethical guidelines, and regulatory requirements relevant to clinical trials.
• Experience with patient-facing responsibilities such as informed consent discussions, recruitment, retention, and participant follow-up.
• Proficiency in data entry, data quality review, and basic use of electronic data capture or clinical trial management systems.
• Effective communication and collaboration skills for working with investigators, site staff, monitors, sponsors, and ethics committees.
• Strong organizational and time-management abilities, with attention to detail and capability to handle multiple studies or tasks simultaneously.
• Bachelor’s degree in life sciences, pharmacy, nursing, or a related field; prior experience as a CRC or in clinical research is preferred.
• Comfort working in an on-site environment in Mysuru, with a commitment to participant safety, data integrity, and continuous learning.