6 Monitoring Visits Jobs

Role Overview: As a Clinical Research Associate at the world's largest and most comprehensive clinical research organization, powered by healthcare intelligence, you will be part of a team that values innovation and continuous improvement. You will work in a collaborative environment that encourages belongingness, empowerment, and reaching your full potential to contribute to saving lives. Key Responsibilities: - Perform all aspects of Clinical Research Associate (CRA) duties, including site selection, site initiation, routine monitoring visits, and close-out visits. - Work closely with the client's study team and receive support from a dedicated ICON line manager. - Oversee study site manag...

As an Officer/Sr. Officer in the Consumer Research Department at our company based in Ahmedabad, your role involves: - Identifying and qualifying potential investigators for research studies. - Collecting necessary documents to assess site/investigator feasibility and obtain approval from authorities. - Training the site study team, maintaining essential documents, and overseeing startup activities and site initiation. - Conducting monitoring visits to ensure compliance with study management, protocol, and other requirements at all assigned sites. - Performing source document verification as per the monitoring plan to maintain accurate and up-to-date trial records. - Coordinating with labs a...

Job Summary RTL/Sr. RTL is responsible and accountable for deliveries of studies allocated to RCO unit, performing end to end study related project management for studies managed in-house with-in agreed timelines, budget and desired quality standards. For Outsourced study, RTL/Sr. RTL will be responsible to provide an efficient Sponsor Oversight and accountable for key deliverables and study success. RTL/Sr. RTL is expected to adhere to required procedures and quality in compliance with Sun Procedural Documents, ICH-GCP and local regulations. Area Of Responsibility Planning and Execution of trials as per agreed timelines, budget and ensuring Quality across processes. Planning and Facilitatin...

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...

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...

As a Clinical Research Associate, you will be part of the world's largest and most comprehensive clinical research organization, driven by healthcare intelligence. You will have the opportunity to work within a supportive partnership, fostering an environment that thrives on innovation and continuous improvement. This role is ideal for individuals seeking a workplace where inclusivity and empowerment are paramount, enabling every team member to achieve their full potential, excel in their performance, and contribute significantly to the mission of saving lives. Your responsibilities will include performing a wide range of CRA duties, starting from site selection and initiation, progressing t...