
Job Overview
Location
Research Triangle Park, North Carolina
Job Type
Full-time
Category
DevOps
Date Posted
June 23, 2026
Full Job Description
đź“‹ Description
- • Lead and direct clinical site management teams throughout the entire lifecycle of clinical trials, from study initiation to closeout
- • Serve as the primary point of contact and representative for clinical monitoring and site activities within assigned projects
- • Act as the main liaison between Worldwide Clinical Trials and sponsor clients, ensuring clear and professional communication
- • Manage all monitoring deliverables to align with study budgets and identify, escalate, or resolve out-of-scope activities
- • Provide strategic oversight and guidance to Clinical Research Associates (CRAs) and other site management staff
- • Ensure compliance with regulatory standards, Good Clinical Practice (GCP), and sponsor-specific protocols across all monitored sites
- • Monitor study progress and timelines, proactively addressing delays or operational challenges to maintain trial integrity
- • Utilize clinical trial management systems (CTMS) and electronic data capture (EDC) systems to track site performance and data quality
- • Collaborate with cross-functional teams including data management, biostatistics, and regulatory affairs to support trial execution
- • Maintain strong customer focus by building and sustaining trusted relationships with sponsor representatives
- • Demonstrate initiative by identifying potential risks and proposing practical, timely solutions to operational obstacles
- • Lead remote teams effectively, ensuring alignment, accountability, and high performance across distributed locations
- • Travel up to 30% to conduct site visits, attend investigator meetings, or support key trial milestones
- • Apply specialized knowledge in central nervous system (CNS) and neurology trials, including Alzheimer’s disease studies
- • Uphold a patient-centric approach, treating every trial as critical to patient outcomes and therapeutic advancement
- • Contribute to a culture of quality, innovation, and ethical research that prioritizes both scientific excellence and human impact
🎯 Requirements
- • Bachelor’s Degree or Nursing Degree required
- • 1+ years’ experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role
- • 3+ years’ experience as a Clinical Research Associate
- • CNS/Neurology trial experience required; Alzheimer’s experience preferred
- • Proficiency in Microsoft Office, CTMS, and EDC systems
- • Ability to lead and motivate remote teams effectively
🏖️ Benefits
- • Annual salary range of $112,000.00 - $222,000.00
- • Competitive benefits package based on location
- • Transparent compensation practices with pay equity commitment
- • Opportunity to work on groundbreaking CNS and neurology clinical trials
- • Supportive, values-driven culture focused on inclusion and professional growth
- • Travel opportunities up to 30% for site visits and meetings
Skills & Technologies
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About Worldwide Holdings Corporation
Worldwide Holdings Corporation is a diversified global enterprise engaged in the development, manufacturing, and marketing of a wide range of products and services. The company operates across various sectors, including technology, consumer goods, and industrial solutions, with a strong focus on innovation and sustainability. Worldwide Holdings Corporation is committed to delivering high-quality products and exceptional customer service, aiming to foster long-term relationships with its clients and stakeholders. The company's strategic vision involves expanding its global reach, investing in research and development, and adapting to evolving market demands to maintain a competitive edge in the international marketplace. Their mission is to create value through responsible business practices and a dedication to excellence.
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