Clinical Research Associate

GLANIS HOSPITAL is a 100 Bed, Rural, Teaching Hospital located in A. Thottiapatti in Madurai district (near Thirumangalam, Madurai). The hospital's mission is to provide low-cost, affordable healthcare to the rural population and high-quality medical education & training to healthcare professionals. GLANIS INSTITUTE OF MEDICAL SCIENCES is an educational &...

Job location Chennai YOUR TASKS AND RESPONSIBILITIES Perform site feasibility identify potential investigator negotiate study budget with potential investigators finalization of investigators sites and execution of CDA and study-related contracts Preparation and submission of study documents for EC permission for respective study across centers ...

**About TruVita Wellness Inc.** TruVita Wellness Inc. is building the future of AI-powered telemedicine through a cutting-edge AI Doctor and smart Telemedicine. We aim to deliver personalized, accessible, and affordable healthcare with technology and empathy at the core. We are looking for a **Clinical Research Physician (MBBS)** who can help us clinically...

Clinical Research Physician - Office based - Chennai ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Clinical Research...

Role DescriptionThis is a full-time on-site role for a Senior Clinical Research Coordinator, located in Chennai. The Clinical Research Coordinator will be responsible for managing clinical trials, ensuring informed consent is obtained, and adhering to research protocols. The role involves coordinating and overseeing day-to-day research activities,...

1. Having an insight regarding the study materials shared and presenting the same to the concerned doctor 2. Completing the documents like Feasibility Questionnaire, Confidentiality Disclosure Agreement, Investigator Undertaking etc.. required for study Start-Up activity. 3.Collection of documents like calibration certificates, lab documents etc.. from the...

Clinical Research Coordinator (CRC) manages and coordinates the day-to-day operations of a clinical trial, which includes recruiting and screening participants, obtaining informed consent, collecting and managing data, and ensuring compliance with study protocols and regulations. They also act as a liaison with sponsors, investigators, and regulatory bodies,...

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines. 3....

Ensure the integrity of data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations, and internal SOPsPrepare and maintain documents related to clinical trials.Generate data entry queries and test clinical applications for numerous clinical trials.Analyze clinical trials data and prepared reports for Data...

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines. 3....