Johnson & Johnson - Salem, OR
posted 4 months ago
Johnson & Johnson is seeking a Manager, Site Contract Management Start Up to join our team in Titusville, NJ. This role may offer remote work options on a case-by-case basis, subject to company approval. The successful candidate will serve as a subject matter expert on Global Clinical Operations (GCO) Clinical Contract Services (CCS) study start-up activities, focusing on cross-functional requirements that impact operational timelines. This position is pivotal in the collection, management, and dissemination of information necessary for developing and executing site budgets, contracts, and payments efficiently and effectively. The candidate will provide customer-focused leadership and collaboration in executing the GCO-CCS operational strategy and managing studies, projects, and programs. In this role, the Manager will act as the primary Point of Contact (POC) within GCO CCS for Global Development partners, supporting end-to-end study start-up activities. The candidate will lead and support functional and cross-functional teams to ensure project timelines are met, maintaining high-quality standards and efficiency. Responsibilities include tracking activities, reporting study status to stakeholders, and providing insights for site selection based on GCO-CCS experience. The Manager will liaise with cross-functional stakeholders throughout the study planning process to ensure contract delivery milestones align with site activation targets. Participation in Cross-Functional Trial Team (CFTT) project meetings, kick-off meetings, and investigator meetings is also required. The role demands establishing and maintaining methods for initiating study start-up planning, utilizing knowledge of clinical trial operations, and having clinical trial contracting experience. The Manager will track study start-up progress, provide regular updates to the GCO CCS management team, and escalate issues as necessary. Additionally, the candidate will support continuous improvement initiatives to enhance processes further. This position is integral to the success of clinical trials and requires a proactive approach to managing multiple projects and priorities effectively.