Clinical Research Co-ordinator -Geron Study St Johns Research Institute

0.0 years

0 Lacs

bengaluru, karnataka, india

On-site

Brief Description About The Project Interaction with Patients, Sponsor/CRO, IEC, Lab staff and other departments in the institution and conduct the study according to ICH GCP Guidelines, SOPs and study protocol guidelines and act as the main line of communication between patients, Investigators and CROs in study conduct activities. Assist in Feasibility questionnaires, Coordinate in pre-site selection visit, site initiation visit. Assist the Principal Investigator and Co investigators in screening of subjects by maintaining and updating the list of potentially eligible patients for the ongoing studies. Clinical Research Co-ordinator No. of Vacancy: Two Preferred Qualifications: Degree with l...

Posted 1 month ago

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Clinical Research Co-ordinator - Analytical St Johns Research Institute

0.0 - 3.0 years

0 Lacs

karnataka

On-site

As a Clinical Research Coordinator at Analytical Project, St. John's Research Institute in Bangalore, your role will involve interaction with patients, Sponsor/CRO, IEC, Lab staff, and other departments in the institution. You will conduct the study according to ICH GCP Guidelines, SOPs, and study protocol guidelines. Your main responsibility will be to act as the main line of communication between patients, Investigators, and CROs in study conduct activities. **Key Responsibilities:** - Coordinate in screening, Audio-Video consenting, enrollment, periodic study visits, and close-out visits. - Ensure that rights and well-being of a research participant are protected throughout the study dura...

Posted 3 months ago

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Clinical Research Co-ordinator St Johns Research Institute

0.0 - 3.0 years

0 Lacs

karnataka

On-site

As a Clinical Research Coordinator at Analytical Project, St. John's Research Institute in Bangalore, you will be responsible for interacting with patients, sponsors, IEC, lab staff, and other departments to conduct studies following ICH GCP Guidelines, SOPs, and study protocol guidelines. You will act as the main communication line between patients, Investigators, and CROs during study conduct activities. **Key Responsibilities:** - Coordinate in screening, Audio-Video consenting, enrolment, periodic study visits, and close out visits. - Ensure the protection of the rights and well-being of research participants throughout the study duration. - Coordinate with finance, legal, and regulatory...

Posted 3 months ago

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