0.0 years

0 Lacs

mumbai, maharashtra, india

On-site

Conduct site/trial feasibility to identify & select the right site and investigator for the study Ensure timely compilation of all essential documents & assist in regulatory package preparation, timely submission, follow up with site EC to resolve any queries, and obtain approvals Ensuring site setup according to protocol, review patient data base & pre-screening, identify physician network Coordinate for Clinical Trial Supplies receipt, accountability & storage Prepare site team for study initiation visit and coordinate with monitor for the visit Assist in the process of administering the informed consent to the potential objects and discussing in detail the patient information sheet Ensure...

Posted 3 days ago

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Study Coordinator - TKA Project St Johns Research Institute Sjri

1.0 - 6.0 years

2 - 5 Lacs

bengaluru, karnataka, india

On-site

Roles and Responsibilities: Participant Coordination & Recruitment Work under the guidance of the Investigator to assist with all study-related responsibilities Conduct and document the informed consent process Educate participants on study procedures, duration, risks, benefits, and compensation Assist in subject enrollment and assign screening codes Maintain follow-up communication with participants Study Conduct & Compliance Ensure strict adherence to GCP , Ethics Committee (EC) guidelines, and the approved protocol Follow the Schedule of Assessments in coordination with the study team Coordinate lab activities: sample collection, processing, packaging, and shipping Ensure subject well-bei...

Posted 2 months ago

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