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
Remote · Eastern Cape, South Africa, Tegucigalpa, Francisco Morazán, Honduras, United States
The Senior Project Manager leads cross-functional teams to deliver Phase I-IV clinical trials from start-up through closeout. They are responsible for managing project timelines, budgets, and quality while serving as the primary point of contact for clients.
On-site
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and…
On-site
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and…
Remote · United States
The Operations Manager oversees rater selection, certification, training content, and scale acquisition for clinical trials. They ensure all project operations comply with SOPs, ICH/GCP, and regulatory guidelines while managing study timelines and budgets.
Remote · United States
The Clinical Scientist is responsible for the review, interpretation, and assessment of clinical data to ensure high-quality reporting and study integrity. They collaborate with cross-functional teams to manage protocol-defined variables, track safety events, and present key findings to clients and medical monitors.
Remote · United States
The RTSM Specialist manages the implementation and decommissioning of RTSM systems, ensuring deliverables meet client requirements and company standards. They serve as the primary escalation point for project issues and oversee study design, budget, and vendor work orders.
Remote · United States
The Executive Director of Project Management oversees the direction of the project management team, including financial performance, resource management, and strategic business acquisition. They are responsible for maintaining effective client relationships, leading sub-therapeutic groups, and ensuring project deliverables meet sponsor expectations.
Remote · Ontario, Canada, Quebec, Quebec, Canada
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and regulatory compliance. They are responsible for overseeing site performance throughout the study lifecycle and ensuring adherence to safety and protocol requirements.
Remote · United States
The Project Manager is responsible for the overall coordination and management of clinical trials from startup through closeout. They lead core project teams and manage technical, financial, and operational aspects to ensure deliverables meet time, quality, and cost expectations.
Remote · United States
The Project Manager is responsible for the end-to-end coordination and management of clinical trials from startup through closeout. They lead cross-functional teams to ensure project deliverables meet time, quality, and cost expectations while implementing contingency plans as needed.
Remote · United States
The Project Manager is responsible for the end-to-end coordination and management of clinical trials from startup through closeout. They lead cross-functional teams to ensure project deliverables meet time, quality, and cost expectations while implementing rescue strategies when necessary.
Remote · Ontario, Canada
The Senior Clinical Research Associate manages research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements and safety reporting while conducting study initiation visits.
Remote · 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.
Remote · 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.
Remote · 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.
Remote · 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.
Remote · 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.
Remote · 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.
