Clinical Trials Associate

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...

As a Clinical Research Associate, you will be responsible for managing and monitoring clinical trials. You will work closely with investigators to ensure that all aspects of the study are conducted according to protocol and in compliance with regulatory requirements. Your tasks will include preparing and reviewing study documents, ensuring adherence to...

As a Clinical Research Associate, you will be responsible for managing and monitoring clinical trials. You will work closely with investigators to ensure that all aspects of the study are conducted according to protocol and in compliance with regulatory requirements. Your tasks will include preparing and reviewing study documents, ensuring adherence to...

Senior Data Scientist Job DescriptionThis role involves overseeing the development and implementation of clinical trial platform technologies, ensuring seamless integration with existing systems.We are seeking a highly skilled Data Scientist to support our team in decision-making by providing analytical insights and identifying patterns.The ideal candidate...

**Job description** - Manage Clinical & Non-Clinical study portfolios - design & develop protocols along with other clinical trial documents & reports that fit with the regulatory pathway and standards - Responsible for planning, scheduling and implementing the clinical aspects of projects in-line with Monitoring Plan, Recruitment Plan, Clinical Training...

Job OverviewAs a Central Monitor Professional, you will contribute to the success of global clinical trials by delivering high-quality results within specified timelines and budgets. This role may involve leading specific aspects of the trial process and contributing to operational excellence through process improvement and knowledge sharing.Key...

JOB DETAILS 1.Collaborating with Project Manager to set targets for clinical monitoring staff, and ensuring recording of trial in compliance with project goals.2.Creating and implementing study-specific clinical monitoring tools and documents.3.Creating and overseeing trial budget.4.Identifying, enlisting and choosing sites, and coordinating site management...

Job DescriptionResponsible for supporting, under the guidance of the Lead Clinical Trial Leader and/or Clinical Trial Leader (CTL) and the Clinical Program Leader (CPL), all aspects of TCO clinical trial(s) as assignedMajor accountabilities:- May lead studies in maintenance or in closeout phase or ongoing studies post primary database lock with the oversight...

Job Title: Clinical Trials Vendor ManagerAbout the Role:We are seeking a highly skilled Clinical Trials Vendor Manager to join our team. The ideal candidate will have experience in managing vendors for clinical trials and pharmacovigilance processes.The successful candidate will be responsible for ensuring that vendors meet all worldwide regulatory authority...

About the RoleAs a Clinical Trial Submission Management Specialist, you will be responsible for ensuring Clinical Trial Application approvals in the EU throughout the whole study lifecycle. This involves working closely with cross-functional teams to ensure compliance with EU regulations and guidelines.Key responsibilities include preparing submission...