Senior Clinical Trial Manager

Company Description CureNet Research is a national clinical research organization that supports physician-led sites with infrastructure, training, and technology to participate in clinical studies. The company partners with physicians, research sites, and sponsors to facilitate high-quality study execution and broaden access to research across a network of independent practices. CureNet provides comprehensive site support through all stages of study participation, including start-up, feasibility, budget and contract negotiation, IRB coordination, regulatory processes, and ongoing operations. With centralized SOPs, GCP/ICH training, and integrated technology, CureNet builds compliant, research-ready environments that maintain agility while ensuring structure and consistency. Built around a physician-led model, CureNet focuses on expanding access to clinical research and supporting the long-term success of independent practices.

Role Description The Senior Clinical Trial Manager will oversee the planning, execution, and oversight of clinical trials across CureNet’s network of physician-led research sites. This contract, remote role includes leading trial start-up activities, coordinating feasibility assessments, and ensuring timely completion of regulatory submissions and IRB approvals. The individual will manage site performance, monitor trial progress against timelines and budgets, and collaborate with investigators, site staff, sponsors, and CRO partners to resolve operational issues. Day-to-day responsibilities include reviewing protocols for operational feasibility, implementing risk management and quality oversight plans, and ensuring adherence to SOPs, GCP/ICH guidelines, and regulatory requirements. The Senior Clinical Trial Manager will also support training and mentoring of site and project staff, contribute to continuous process improvement, and provide clear reporting and documentation for stakeholders.

Qualifications

• Candidates should possess strong skills in Trial Management, including planning, execution, and oversight of multi-site clinical studies.
• Candidates should possess expertise in Clinical Operations, including site coordination, timelines, budgets, and quality and risk management.
• Candidates should possess proficiency with Protocol review and implementation, ensuring operational feasibility and compliance with study requirements.
• Candidates should possess experience in Clinical Trials, including phase II–IV or post-marketing studies, and familiarity with sponsor and CRO collaboration.
• Candidates should possess solid Research skills, including understanding of GCP/ICH guidelines, regulatory processes, and ethics committee/IRB coordination.
• Advanced knowledge of regulatory requirements and SOP-driven environments; experience with centralized and remote trial oversight is beneficial.
• Strong communication, stakeholder management, and problem-solving skills; ability to work independently in a remote setting and manage multiple priorities.
• Bachelor’s degree in a life science or related field required; an advanced degree (e.g., MS, MPH, PharmD, MD, or equivalent) or clinical research certification (e.g., ACRP, SOCRA) is an advantage