Clinical Trial Executive

Job OpportunityA seasoned Clinical Research Specialist is required to oversee trial protocols, establish and manage clinical sites, train staff on therapeutic areas, and ensure compliance with regulatory standards.Key Responsibilities:Develop and execute trial protocols for steering committeesIdentify, evaluate, and set up clinical trial sitesTrain site...

Clinical Research Manager Job Description About the Role The Clinical Trial Manager will oversee clinical monitoring staff, ensuring trial compliance with project goals. They will create and implement study-specific clinical monitoring tools and documents. Main Responsibilities Collaborate with Project Managers to set targets for clinical monitoring staff....

Associate/Content Editor in the Clinical Trials team We are looking for an Associate Content Analyst/Content Analyst to join our Clinical Trails team in Hyderabad/Chennai/Bangalore. This is an amazing opportunity to work on Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. We have a great skill set in Clinical and we would...

Clinical Research AssociateJob Description:We are seeking a highly skilled Clinical Research Associate to join our team. The successful candidate will be responsible for managing clinical trials from start to finish, ensuring that all trials are conducted in accordance with Good Clinical Practice (GCP) guidelines and regulatory...

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...

JOB DETAILS 1.Creating and writing trial protocols, and presenting these to steering committee.2.Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3.Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4.Liaise with ethics committee...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Integrity, Collaboration, Agility...

TMF Specialist Job OverviewWe are seeking a highly skilled professional to fill the role of TMF Specialist within our Clinical Operations group. This position will play a vital part in ensuring the seamless execution of clinical trials, collaborating closely with cross-functional teams.Key Responsibilities:Process study documents in accordance with client...

JOB DETAILS 1.Creating and writing trial protocols, and presenting these to steering committee.2.Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3.Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4.Liaise with ethics committee...

**Job description** **Role & responsibilities**: - Overseeing the collection, validation and processing of clinical trial data. - Developing and implementing data management procedures for clinical trials. - Supporting and facilitating the review of medical coding for validity and completeness. - Ensuring compliance with applicable regulations, protocols...