Job Overview
Location
Durham, North Carolina
Job Type
Full-time
Category
Product Management
Date Posted
June 23, 2026
Full Job Description
đź“‹ Description
- • Manage research activities at clinical trial sites participating in Worldwide’s oncology-focused clinical research projects
- • Engage in all stages of clinical studies, including identifying and selecting potential trial sites
- • Perform study start-up activities such as collecting and verifying regulatory documents from sites, supporting contract and budget negotiations, and ensuring site readiness
- • Conduct study initiation visits (SIVs) to train site staff on protocol requirements, data collection procedures, and safety reporting protocols
- • Monitor site compliance with informed consent processes, regulatory standards, and Good Clinical Practice (GCP) guidelines
- • Oversee site performance during study maintenance, ensuring timely and accurate data entry and resolution of queries
- • Close out research activities at sites upon study completion, including final documentation and regulatory file reconciliation
- • Perform most site management duties remotely, with required regional travel to conduct on-site monitoring as needed
- • Ensure accurate and timely reporting of potential safety-related events in accordance with regulatory requirements
- • Collaborate with in-house Clinical Research Associates and regulatory teams to support complex site management needs
- • Maintain proficiency in Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) systems
- • Utilize strong organizational skills to manage multiple sites and study timelines with minimal supervision
- • Communicate effectively with site personnel, sponsors, and internal teams through written and oral English communication
- • Adhere to all applicable federal, state, and international regulatory requirements for clinical research
- • Contribute to a team-oriented culture focused on patient outcomes and scientific excellence in oncology clinical trials
- • Participate in regular coaching and development conversations with Line Manager to support career progression toward Clinical Trial Manager roles
🎯 Requirements
- • 2 - 5 years of experience as a regional, traveling Clinical Research Associate
- • 4-year university degree OR Nursing Degree
- • Experience in Oncology is required
- • Willingness to travel regionally required
- • Proficiency in Microsoft Office, CTMS, and EDC Systems
- • Excellent interpersonal, oral, and written communication skills in English
🏖️ Benefits
- • Annual salary range of $79,500.00 - $158,500.00
- • Competitive benefits package depending on location
- • Transparent compensation and pay equity practices
- • Clear career path with opportunities to advance to Clinical Trial Manager roles
- • Supportive, team-oriented environment with accessible leadership
- • Emphasis on professional development through regular coaching and feedback
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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