Senior Statistical Programmer in 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...

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...

Senior Legal Manager for Clinical TrialsWe are seeking an experienced Senior Legal Manager to join our team at Novo Nordisk. As a key member of our Legal and Compliance department, you will play a crucial role in ensuring compliance with laws, regulations, and internal policies for clinical trials.About the Role:Ensure compliance with laws, regulations, and...

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 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...

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 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...

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...

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...

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...

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,...

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...

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.

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 SummaryWe are seeking a skilled and detail-oriented Global Clinical Trials Coordinator to join our team. As a key member of our clinical operations group, you will play a critical role in supporting the coordination and execution of clinical trials.About the RoleThis position is responsible for providing administrative and technical support to project...

About ICON PlcICON Plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment that drives innovation and excellence, where we welcome talented individuals to join our mission in shaping the future of clinical development.Salary InformationWe offer a competitive salary ranging from $80,000 to $120,000...

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...

At ICON Plc, our success relies on exceptional professionals like you.We're driven by a shared vision to advance and improve patients' lives through innovative clinical research solutions.As Clinical Trials Project Lead, you will play a vital role in the delivery of all clinical aspects of our studies, ensuring timely completion and exceeding customer...

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...