By admin 
Clinical Research Associate
Job description
· Conduct site selection, initiation, routine monitoring, and close-out visits to research sites participating in clinical trials
· Ensure that study sites are following the study protocol, GCP, and applicable regulatory guidelines
· Perform source data verification and data quality checks to ensure accuracy and completeness of study data
· Monitor subject enrollment, adherence to inclusion/exclusion criteria, and overall study progress
· Collect, review, and maintain essential study documents, including regulatory submissions and informed consent forms
· Communicate effectively with investigators, site staff, and study sponsors to address queries, provide guidance, and resolve issues
· Identify and report adverse events and protocol deviations, ensuring appropriate follow-up and documentation
· Assist in the preparation and conduct of site audits and inspections by regulatory authorities and sponsors
· Collaborate with cross-functional teams, including project managers, data managers, and medical monitors, to ensure smooth study execution
· Maintain accurate and up-to-date study tracking, monitoring, and reporting documentation
· Participate in study team meetings and contribute to study planning, protocol development, and study-related activities
Minimum Qualifications & Experience:
Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered. Must have good time management skills, attention to detail, be able to work well in a team, and be computer literate. Preferably experience of working in the research, pharmaceutical industry or a related field per job level as follows:
Approximately 2-3 years of Clinical Research Associate experience or equivalent experience in other roles in the Clinical industry.
Place: Bangalore
Interested candidates can send your resume to
Dr. C.T. Sadashiva:
rndstarhiherbs@gmail.com
research@starhiherbs.com
mobile–9342575028