Lead Clinical Trial Data Analyst

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...

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...

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...

Senior Clinical Research Coordinator Job DescriptionAbout Us:We are a fast-growing Clinical Trials Organization dedicated to providing high-quality, ethical, and efficient clinical trial services. We are committed to excellence in research and uphold the highest standards of regulatory compliance and data integrity.Job Summary:We are seeking an experienced...

Job Title:Clinical Trials CoordinatorWe are seeking a skilled professional to support the management of clinical trials. As a key member of our team, you will be responsible for ensuring compliance with regulatory requirements and coordinating submissions in various systems.Main Responsibilities:Assignments: Be assigned to one or more projects under...

Job Description">As a key player in our team, you will leverage your expertise to provide exceptional support to external suppliers, ensuring their effectiveness in delivering clinical trials for our study teams. This vital role involves working closely with internal and external stakeholders to resolve technical issues quickly, perform root cause analysis,...

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...

Job Description SummaryClinical Trial Supply Manager (CTSM) defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management to ensure supply continuity to patients.The CTSM is the GCS single point of contact at trial level for the respective core CTT (Clinical trial team) and/or CTT Sub-Team they...

Job Description Summary Clinical Trial Supply Manager (CTSM) defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management to ensure supply continuity to patients.The CTSM is the GCS single point of contact at trial level for the respective core CTT (Clinical trial team) and/or CTT Sub-Team they...