Apollo Research and Innovations

Chennai, Tamil Nadu

Position: Clinical Research CoordinatorQualification Bio Science (B.Pharm/Bio Tech etc.)Experience Above 1 Year (Clinical Research Experience must) Timing General ShiftSalary 2L 2.5L (Per annum)Location Visakhapatnam/Chennai/BangaloreLanguage Know English/Kannada/TeluguJOB Description Clinical Research Coordinator To have the good knowledge of regulations and GCP guidelines. Ability to communicate properly between the physician, patient & the site head. Assist Senior CRC in Screening including informed consent process, randomization, enrolment & follow-up (including Telephonic Follow-up) process & procedures. Maintenance of Investigator Master File as per Good documentation practices & SOP including generation of source documents. Present in Site Initiation Visit, Monitoring Visits, Site Closeout Visit. CRF, e-CRF entry, Data Query resolution. Coordinate between the local/Central laboratory and courier for the shipment. Assist the pharmacist in drug accountability and temperature maintaining logs. Assist the Sr. CRC in maintaining the accountability of study materials and in scheduling study procedures. Endow the required file notes, weekly and monthly and monthly report to the reporting authority. Tracking the status of all study activities. Report Sr.DGM daily and take advice for further action.

Position Clinical Research CoordinatorQualification B.PharmExperience - Above 1YearsTiming - General ShiftSalary Based upon PerformanceLocation ChennaiLicence: Pharmacy Lice(Only B. Pharm is eligible for this Job)Job Description Clinical Research Coordinator: To have the good knowledge of regulations and GCP guidelines. Ability to communicate properly between the physician, patient & the site head. Assist the Site Head in the managing the Site to ensure ethical conduct of research activities. Assist Site Head in evaluates protocols, policies and procedures regarding research projects and studies. Maintains pertinent records and documentation. Provide guidance to CRC in Screening including informed consent process, randomization, enrolment & follow-up (including Telephonic Follow-up) process & procedures. Maintenance of Investigator Master File as per Good documentation practices & SOP including generation of source documents. Oversight of Site Initiation Visit, Monitoring Visits, Site Closeout Visit. CRF, e-CRF entry, Data Query resolution. Assist the pharmacist in drug accountability and temperature maintaining logs. Monitoring Sr. CRC and CRC in maintaining the accountability of study materials and in scheduling study procedures. Endow the required file notes, weekly and monthly and monthly report to the reporting authority. Tracking the status of all study activities. Report to the Site Head daily and take advice for further action. Delegate the work to Senior/Junior/Trainee CRCs as per the requirement.Job Types: Full-time, PermanentSalary: ?10,000.00 - ?15,000.00 per month