Worldwide Clinical Trials is a global contract research organization that partners with biopharmaceutical companies to deliver customized solutions for clinical trials and drug development.
Research Triangle Park, NC
Worldwide Clinical Trials (Worldwide) is a global CRO serving development-driven biopharmaceutical companies, with more than 4,400 professionals operating across more than 70 countries. The company delivers therapeutically dedicated expertise in neuroscience, oncology, rare disease, and internal medicine, with comprehensive support across every development phase – from early-stage and first-in-human studies through Phase III registration trials. The company's flexible service model – spanning full-service trial management to functional service partnerships through Worldwide Flex – is powered by a people first, partnership driven outsourcing approach that strengthens collaboration, enhances data transparency, and supports more informed decision making. This provides sponsors with tailored, adaptable solutions that keep pace with the evolving demands of clinical research. Learn more at www.worldwide.com
Télétravail · Canada, United States
The Director will oversee the delivery of clinical projects within cost, time, and quality requirements while providing direct supervision and mentoring to project managers. They will also collaborate with the Business Development team on proposals and contribute to the continuous improvement of business processes.
Télétravail · United States
The Site Identification and Relationship Manager will lead post-award site identification strategies, including feasibility management and outreach coordination. They are also responsible for training assigned resources and overseeing Site Activation Specialist support activities.
Télétravail · Canada, United States
The Senior Project Manager coordinates clinical trials from start-up through closeout, managing technical, financial, and operational aspects. They collaborate with functional leads to ensure all project deliverables meet customer time, quality, and cost expectations.
Télétravail · Canada, United States
The Project Manager is responsible for the overall coordination and management of clinical trials from start-up through closeout. This includes directing technical, financial, and operational aspects to ensure deliverables meet customer time, quality, and cost expectations.
Télétravail · Quebec, Quebec, Canada
Manage research activities at clinical sites, including site identification, start-up activities, and study maintenance. Conduct site initiation visits and ensure compliance with regulatory requirements and safety reporting.
Télétravail · United States
Accountable for directing multiple clinical projects simultaneously to ensure delivery within cost, time, and quality requirements. Acts as a liaison for business development and collaborates across functional areas to improve business processes.
Télétravail · Canada, United States
The role involves providing operational oversight and resource management for Clinical Assessment Technologies (CAT) study projects. Key duties include managing study deliverables, coordinating with vendors, and contributing to business development activities and process improvements.
Télétravail · United States
The role involves acting as a GCP Subject Matter Expert to ensure study protocol compliance and managing root cause analysis for quality issues. The lead will also perform quality reviews, support site inspections, and manage the QA relationship with sponsors.