Senior Legal Manager for Clinical Trials

About the RoleWe are seeking a skilled and detail-oriented Global Clinical Trials Operations Coordinator to join our team at Worldwide Clinical Trials. In this role, you will play a critical part in ensuring the smooth operation of our clinical trials.

About the RoleWe are seeking a Clinical Trials Senior Analyst to join our team in Mexico. As a key member of our clinical development department, you will be responsible for ensuring compliance with importation and exportation laws.The successful candidate will have at least 3 years of experience as a Clinical Trials Assistant, preferably working with...

About the RoleWe are seeking a Senior Clinical Development Manager to lead and manage our global investigator engagement team. As a key member of our clinical development organization, you will be responsible for ensuring the timely execution of clinical trials across all therapeutic areas.Your primary focus will be on collaborating with business partners to...

Job Title: Clinical Trial Associate II, TMF Operations SpecialistJob Summary:We are seeking a highly organized and detail-oriented Clinical Trial Associate II, TMF Operations Specialist to join our team at Worldwide Clinical Trials. In this role, you will be responsible for processing, maintaining, and archiving all essential documents in compliance with...

Job DescriptionWe are seeking a Clinical Assessment Expert to join our team at Worldwide Clinical Trials. This role is responsible for all aspects of assigned projects that include clinical assessment, training development, and data review.Key Responsibilities:Assist in the review of eCOA/ePRO specifications and engage in User Acceptance Testing of equipment...

Company OverviewAt ICON, we're a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment that drives innovation and excellence. Our mission is to shape the future of clinical development.About the RoleWe're seeking a Senior Centralized Clinical Trial Manager to oversee and optimize centralized clinical...

Contract Analyst I Job DescriptionAt Icon PlcWe are seeking a skilled Contract Analyst I to play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Key Responsibilities:Review and analyze contracts, agreements, and legal documents related to...

At Thermo Fisher Scientific, we are seeking a highly skilled Operations Coordinator to support our clinical trials team. This role is ideal for an individual who is detail-oriented, organized, and able to work effectively in a fast-paced environment.**Job Summary:**The Operations Coordinator will be responsible for coordinating and overseeing various tasks...

Job SummaryThe Administrative Coordinator for Clinical Research is responsible for providing administrative support to the project team in the execution of clinical trials. This role will work closely with the Project Manager and other team members to ensure the timely completion of tasks and meet client expectations.

Thermo Fisher Scientific is seeking a highly skilled and experienced Senior Clinical Research Associate to join our team. As a Senior Clinical Research Associate, you will be responsible for ensuring compliance with clinical trials across various regions.

About the RoleWe are seeking a skilled Clinical Payments Specialist to join our team at Worldwide Clinical Trials. As a Clinical Payments Specialist, you will be responsible for the end-to-end management of global Investigator payments for assigned studies.Key ResponsibilitiesManage the set-up, deployment, and close-out of study payments solutionsPerform...

GSK seeks a highly skilled Strategic Regulatory Expert to lead the set-up and execution of regulatory strategies for clinical trials across all therapeutic areas. As a key member of our team, you will be responsible for providing support in achieving the Study Start-up process.Responsibilities:Coordinate planning, start-up, and maintenance of regulatory...

Job DescriptionWe are seeking a highly skilled Associate, Accounts Receivable to join our team at Worldwide Clinical Trials.Job Summary:Prepare and render invoices to sponsors/clients for services, pass-through cost reimbursements, and grants.Maintain and reconcile billing, accounts receivable, and related reports.Reconcile unbilled services/reimbursable...

At ICON plc, we are seeking a skilled Senior Study Start Up Associate to join our dynamic team. This role will involve working within a large-scale, fast-paced environment, supporting the Study Start Up Team Lead in developing and executing the plan for country and site distribution.Your expertise and dedication will be essential in efficiently conducting...

About the RoleWe are seeking a highly skilled and experienced Senior Clinical Trials Project Lead to join our team at ICON plc, a world-leading healthcare intelligence and clinical research organisation.The successful candidate will be responsible for delivering all clinical aspects of the study, overseeing the clinical portion of the budget, developing...

About the OpportunityThis is a chance to take your career to new heights at Signant Health, a global leader in evidence-generation for clinical trials. We're driving change through technology and innovations that meet patients where they are.Job DescriptionWe're looking for an experienced Senior Project Lead to manage projects from planning to completion,...

Job SummaryWe are seeking a seasoned Clinical Quality Assurance Manager to join our team at Icon Plc, a world-leading healthcare intelligence and clinical research organization.About the Role:The successful candidate will play a pivotal role in ensuring the quality and compliance of clinical trials, interpreting regulatory requirements, and contributing to...

At Fortrea, a leading global contract research organization (CRO), we're seeking a skilled Clinical Document Specialist to join our Clinical Pharmacology Services team. This exciting opportunity allows you to contribute to the development of life-changing therapies and treatments while working in a dynamic, remote environment.The ideal candidate will be...

Syneos Health is a leading biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.Our company culture is based on teamwork, with every role vital to furthering our vision of Shortening the Distance from Lab to Life....

Job Description:We are seeking a skilled professional to support the processing, maintenance, and archiving of essential documents in compliance with industry standards. Key responsibilities include performing lead activities, supporting setup, maintaining resources, and providing subject matter expert support.About Worldwide Clinical Trials:Worldwide...