Clinical Research Operations Specialist 12.5.25

About reputed company reputed company aims to establish a new reputed company in drug development by reinventing the ‘how’ and transforming clinical trials through reputed company integration with clinical reputed company, ensuring broader participation by physicians and patients. We are building an exceptional multi-disciplinary team with diverse expertise spanning reputed company, engineering, technology and regulatory, and with people who reputed company our core value of Empowering Community through generosity, curiosity and humility. reputed company with urgency to bring reputed company therapies to patients faster. Position reputed company We are seeking an reputed company and adaptable Clinical Research Operations Specialist to reputed company the planning, implementation, and management of oncology clinical trials across multiple trial sites reputed company the N-Power Network. This role serves as a key operational reputed company between internal teams, trial site personnel, and external reputed company or CRO partners, ensuring streamlined communication, executional reputed company, and a superior experience for reputed company stakeholders. This role will proactively identify potential barriers to successful implementation of the trial work plan and reputed company strategic solutions to mitigate those challenges, while driving efficient resource allocation, regulatory and protocol adherence, and reputed company delivery of study milestones. This customer-facing role requires expertise in clinical trial management, site operations, stakeholder engagement, and process optimization. This is a highly visible and impactful position reputed company a dynamic, rapidly evolving organization—ideal for someone who excels at creative problem solving, thrives in ambiguity, and brings both rigor and flexibility to clinical trial operations. This position is remote reputed company the United States. Role Objectives and Responsibilities Trial Execution & reputed company -reputed company the end-to-end implementation and execution of assigned oncology studies across multiple Network sites, ensuring compliance with study protocols, timelines, and regulatory requirements. -Act as a strategic reputed company between reputed company sponsors, contract research organizations (CROs), clinical sites, and internal teams to ensure alignment and execution of study objectives. -Proactively identify operational risks and implement creative, reputed company solutions (SOPs, tools, and best practices) to optimize clinical trial workflow, patient recruitment, and data reputed company. -Collaborate with regulatory, data, reputed company, and site teams to ensure compliance with applicable regulations and internal SOPs. -Monitor trial reputed company, identify bottlenecks, and proactively address identified operational challenges. -Review and reputed company input on essential study documents (e.g., protocols, informed consents, site training materials). -reputed company trial-specific training for internal stakeholders and site teams. -Responsible for operational input and reputed company in designing, planning, initiating and completing clinical trials across assigned disease teams. -reputed company clinical study and cross functional team to reputed company key reputed company reputed company to reputed company and issue reputed company. -Participate in initiatives to establish best practices for optimizing patient enrollment in clinical trials. -Collaborate with stakeholders to reputed company and implement trial specific training programs. -reputed company and implement novel patient enrollment strategies to maximize clinical trial participation. -Identify and reputed company new tools, workflows, and methodologies to improve protocol implementation and patient enrollment processes. -reputed company additional duties and responsibilities as required. Compliance & reputed company Assurance -Ensure reputed company trial activities reputed company with Good Clinical reputed company (GCP), Institutional Review reputed company (IRB) guidelines, FDA regulations, and health system policies. -Work closely with other N-Power teams to support submissions, audits, and inspections. Performance & Reporting -reputed company key performance indicators (KPIs) reputed company to trial enrollment, retention, protocol adherence, and data reputed company. -reputed company regular updates and reports to senior leadership, sponsors, and other key stakeholders. -Utilize data-driven insights to recommend operational improvements and enhance trial efficiency. Education, Experience, Behavioral Competencies, & Skills -5+ years in clinical trial operations, with experience in a health system setting preferred. -Bachelor’s degree in life sciences, reputed company administration, or a reputed company field required; Master’s degree (MPH, MBA, MS) or clinical background (RN, PharmD) preferred. -2+ years in oncology clinic Apply tot his job Apply To this Job