Global Clinical Trials Coordinator Specialist

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 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...

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...

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...

**About Us**At Worldwide Clinical Trials, we're a global midsize Contract Research Organization (CRO) that pushes boundaries, innovates, and invents to find cures for the world's most persistent diseases.We believe everyone plays an important role in making a difference for patients and their caregivers. Our mission is to work with passion and purpose every...

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...

Company OverviewICON plc is a world-leading healthcare intelligence and clinical research organisation, dedicated to advancing clinical research. From molecule to medicine, we provide outsourced services to pharmaceutical, biotechnology, medical device, and government and public health organisations.We are committed to accelerating the development of drugs...

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...

Role SummaryWe are seeking a skilled Clinical Trials Operations Specialist to join our team, responsible for the global site activation process. This role will ensure seamless execution of clinical trials by collaborating with investigators, sites, and internal stakeholders.About the JobThe ideal candidate will have a scientific or technical degree in...

Company OverviewAt Thermo Fisher Scientific, we are at the forefront of getting cures to market. Our team brings a high caliber of scientific and clinical expertise to the development of drugs that address the world's most challenging health concerns.We know that meaningful results not only require the right approach, but also the right people. We invite you...

Job DescriptionWe are seeking a highly skilled Global Clinical Trial Coordinator to join our team as a Country Approval Specialist. In this role, you will be responsible for preparing, reviewing, and coordinating local EC submissions in alignment with our global submission strategy.You will work closely with internal functional departments to ensure various...

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...

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...

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.

We are seeking a highly skilled Clinical Trials Senior Lead to join our team at Novo Nordisk. As a key member of our Clinical Development department, you will be responsible for ensuring compliance with importation and exportation laws, maintaining close communication with CDC TMs, and anticipating potential risks to avoid them.Key Responsibilities:Be the...

Boston Scientific CorporationWe are a leading medical technology company, and we are seeking a talented Global Clinical Development Specialist to join our team.About the Role:The successful candidate will be responsible for assisting in site selection, qualification, and initiation processes for clinical trials. This includes being the key contact with...

About the RoleWe are seeking a skilled Clinical Trial Coordination Specialist to join our team at Thermo Fisher Scientific. As a key member of our clinical trial operations, you will play a crucial role in ensuring the successful execution of clinical trials.

Job Summary:We are seeking a Clinical Trial Specialist with expertise in regulatory compliance to join our team at Thermo Fisher Scientific. As a Clinical Trial Specialist, you will be responsible for ensuring the seamless execution of clinical trials while adhering to regulatory requirements and company standards.

Unlock Your Potential in Clinical ResearchIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are a diverse, global team that shares a passion for collaboration and solving complex problems.As a Study Start-Up Manager, you will play a critical role in the execution...

At Icon Plc, we're driven by a passion to advance and improve patients' lives. Our diverse teams enable us to become a better partner to our customers, and we're committed to delivering excellence at every touch-point.We foster an inclusive environment where everyone feels valued and empowered to make a meaningful impact. As a Clinical Research Coordinator -...