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

About This OpportunityWe are seeking a skilled Clinical Assessment Technologist to join our team at Worldwide Clinical Trials. This role will be responsible for all aspects of assigned projects, including clinical assessment, training development, and data review.Key ResponsibilitiesAssist in reviewing eCOA/ePRO specifications and engaging in User Acceptance...

At ICON plc, we're seeking a skilled Clinical Trials Specialist to join our dynamic team. As a key member of our team, you will 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,...

Job Title: Senior Regulatory Affairs Specialist With Experience In Clinical TrialsJob Summary:We are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team at ICON plc. As a Senior Regulatory Affairs Specialist, you will play a critical role in ensuring regulatory compliance and facilitating the successful execution of clinical...

Unlock Your Potential in Clinical TrialsAt Amgen, we're dedicated to developing innovative treatments that improve the lives of patients worldwide. As a Local Trial Manager, you'll play a critical role in leading the conduct of clinical trials from start to finish, ensuring the highest quality and scientific integrity.Key Responsibilities:Partner with global...

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...

Job Title: Senior Regulatory Affairs Specialist with Experience in Clinical TrialsWe are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team. As a Senior Regulatory Affairs Specialist, you will play a critical role in ensuring regulatory compliance and facilitating the successful execution of clinical trials.Key...

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 Title: Associate II, TMF OperationsWe are seeking a highly organized and detail-oriented Associate II, TMF Operations to join our team at Worldwide Clinical Trials. As a key member of our operations team, you will be responsible for the processing, maintaining, and archiving of essential documents in compliance with relevant Standard Operating...

About the RoleThe Team Lead, TMF Operations at Worldwide Clinical Trials is responsible for ensuring Trial Master Files are inspection-ready and compliant with relevant Standard Operating Procedures, ALCOA principles, country regulations, and industry best practices.Key ResponsibilitiesDrive the delivery of Project Team objectives in managing essential...

Job Title: Senior Associate I, TMF OperationsWe are seeking a highly skilled Senior Associate I, TMF Operations to join our team at Worldwide Clinical Trials. As a key member of our operations team, you will be responsible for the processing, maintaining, and archiving of essential documents in compliance with relevant Standard Operating Procedures, ALCOA...

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...

About Thermo Fisher Scientific Inc.We are a world-class company that is at the forefront of enabling customers to make the world healthier, cleaner, and safer. As a global leader in serving science, we are committed to providing exceptional solutions that accelerate research, solve complex scientific challenges, drive technological innovation, and support...

**Job Summary:**We are seeking an experienced Clinical Trials Project Lead to join our team in Mexico City. As a Clinical Trials Project Lead, you will be responsible for managing projects in accordance with Good Clinical Practice, ICH, and GCP regulations.About ICON:ICON plc is a world-leading healthcare intelligence and clinical research organization. We...

**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...

Key Responsibilities:- Develop and execute regulatory strategies to support clinical trials, collaborating closely with cross-functional teams and external partners.- Provide comprehensive regulatory guidance and advice to internal and external stakeholders, ensuring compliance with relevant laws and regulations.- Collaborate with project teams to design and...

Clinical Document Specialist OpportunityFortrea is seeking a Clinical Document Specialist to join the global Clinical Pharmacology Services team. This role involves working with project teams to maintain and archive documents produced during clinical trials.Key ResponsibilitiesResponsible for general maintenance and archival of documents produced by study...

Job SummaryThermo Fisher Scientific is seeking a highly motivated and detail-oriented Clinical Trials Coordinator (Level II) to join our team. In this role, you will provide support for clinical trials, medical research, and health care projects.Work Schedule: Flexible schedule to meet the needs of the team and projects.Environmental Conditions: Office...

As a Clinical Trials Project Coordinator at Novo Nordisk, you will be responsible for overseeing the lifecycle management of clinical and real-world evidence Investigator Sponsored Studies (ISS), ensuring seamless coordination from project initiation to completion.**Key Responsibilities:**Manage Research Grants Committee ISS review meetings by sending...