Global Clinical Process Leader

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 Title: Senior Clinical Operations LeadAs a Senior Clinical Operations Lead, you will co-lead the clinical trial team with the study director, overseeing multiple global studies. You will promote learning, sharing, consistent performance, and operational excellence through an agile mindset and team of teams model.Key Responsibilities:Co-lead the clinical...

Job Description:We are seeking a highly skilled Clinical Trial Supply Chain Professional to join our team.The successful candidate will be responsible for leading the study supply strategy, ensuring timely planning and execution of clinical finished goods supply to patients.They will work closely with cross-functional teams to develop and implement optimal...

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...

As part of a study team, participates in processing and quality assurance checks of clinical trial data to ensure data integrity and consistency. Has direct contact with the trial sponsors and internal and external team members. Performs established processing techniques across multiple imaging modalities using proprietary and third-party package software.

As a senior leader in clinical trials, you will play a pivotal role in driving operational excellence and promoting learning within the team. Key responsibilities include co-leading the clinical trial team with oversight from the study director and community lead, as well as ensuring timely delivery of multiple global studies.To be successful in this role,...

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:We are seeking a skilled Medical Writer to join our team. As a Medical Writer, you will be responsible for creating high-quality clinical and safety documents that meet regulatory requirements.You will author and review CSR, DSUR, RMP documents.You will lead outsourced Narrative projects and coordinate other outsourced activities in RWS.You...

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...

Key Responsibilities:Maintain and update cost accounting master data, including standard costs and other processes.Ensure accurate and timely intercompany transactions, including customer and vendor setup and maintenance.Prepare and process intercompany billing and transfer price adjustments.Collaborate with external service providers to coordinate and...