
Job Overview
Location
Research Triangle Park, North Carolina
Job Type
Full-time
Category
Project Manager
Date Posted
May 17, 2026
Full Job Description
📋 Description
- • Senior Project Manager is responsible for the end-to-end coordination and management of clinical trials from start-up through closeout activities, ensuring timely and high-quality delivery.
- • Directs the technical, financial, and operational aspects of clinical projects to secure successful completion in alignment with client expectations and contract obligations.
- • Collaborates with major functional area leads to identify, evaluate, and resolve complex project issues, interpret data, and make sound business decisions that impact project outcomes.
- • Ensures all project deliverables meet customer expectations for time, quality, and cost, acting as the primary point of accountability for project performance.
- • Works closely with Project Management Directors and cross-functional teams to implement proactive, innovative solutions that enhance trial efficiency and client satisfaction.
- • Maintains comprehensive knowledge of project management processes, including budget development, financial tracking, and resource allocation within a CRO environment.
- • Leads and manages multidisciplinary clinical project teams, fostering collaboration among scientists, clinicians, and operational staff across global sites.
- • Applies deep therapeutic area expertise to guide project strategy and decision-making, leveraging Worldwide’s scientific and medical leadership for enhanced trial execution.
- • Utilizes strong communication skills to interface with clients, internal stakeholders, and team members, ensuring clarity, alignment, and transparency throughout the trial lifecycle.
- • Demonstrates ability to perform effectively under pressure, managing competing priorities and high-stakes timelines while maintaining quality standards.
- • Maintains proficiency in essential software tools, including Microsoft Office applications, to support project documentation, reporting, and data management.
- • Contributes to a culture of quality and excellence by adhering to the principle of ‘doing it right the first time’ across all trial phases.
- • Engages in continuous professional growth through immersion in a specific therapeutic area, developing specialized operational and scientific expertise.
- • Represents Worldwide as a trusted partner to clients by delivering reliable, compliant, and patient-centric clinical trial management.
- • Supports a diverse, inclusive, and collaborative workplace culture that empowers employees to thrive and contribute meaningfully to improving patient lives.
- • Travels as required to support client meetings, site visits, or project milestones, ensuring hands-on engagement with global trial operations.
Skills & Technologies
About Worldwide Clinical Trials
Worldwide Clinical Trials is a full-service contract research organization (CRO) specializing in Phase I-IV clinical trials across therapeutic areas including neuroscience, oncology, cardiovascular, immunology, and infectious diseases. Headquartered in Durham, North Carolina, the company provides end-to-end solutions for pharmaceutical, biotechnology, and medical device clients, encompassing clinical development, site management, data analytics, regulatory affairs, and patient recruitment. With a global footprint spanning North America, Europe, Asia-Pacific, and Latin America, Worldwide Clinical Trials leverages technology-driven approaches and a patient-centric model to accelerate drug development. The company emphasizes scientific rigor, operational excellence, and innovation in delivering tailored clinical trial services that support clients from early-phase research through post-marketing surveillance.
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