Director, Clinical Data & Systems

The

Director, Clinical Data and Systems

is responsible for overseeing Data Management services from clinical study initiation through closure, for the Global Clinical Operations portfolio of studies, in accordance with applicable Standard Operating Procedures (SOPs), federal and local regulations, and ICH-GCP guidelines.The Director liaises with internal and external stakeholders, including Contract Research Organizations (CROs) and data vendors, ensuring study data integrity and timeliness of key data deliverables. The Director will support Global Clinical Operations in developing solutions that support data-driven decision making. This is a full-time, remote based position reporting to the Head of Global Clinical Operations. Ideal candidates will be located in the Portsmouth, NH or Chesterbrook, PA Metropolitan areas but we will consider remote candidates anywhere in the United States of America.ESSENTIAL DUTIES AND RESPONSIBILITIES:Accountable for CRO oversight of all outsourced Data Management activities and deliverables and management of internal data activities within Global Clinical OperationsOversee the development and collaboration with internal teams and vendors on all study-level Data Management documentsOversee EDC (and other clinical systems) build and participate in User Acceptance Testing (UAT) for new builds and mid-study updatesAdvise, as a Subject Matter Expert (SME), study team members, including CRO counterparts, and sites on data capture questions and data-related issuesLead internal data analytics and reporting across multiple systemsParticipate in study team meetings (internal and external)Oversee the coordination and facilitation of internal cross-functional data reviewsReview data metrics, perform trend analyses, and escalate concerns/risksProvide cross-functional collaboration and communications to increase data quality and timely data milestonesOversee data imports and merges from multiple systems, correct discrepancies, and ensure qualityCollaborate on the development and maintenance of dashboards to provide data analyticsProvide ad hoc data and report requests in connection with normal business operations, audit requests, and legal and regulatory requirementsEvaluate Data Management key performance indicators and develop action/escalation plans accordinglyMonitor and improve data collection processes; partner to identify how to standardize data across multiple systems; provide recommendations for enriched reporting and data standardsIdentify and communicate lessons learned, best practices and frequently asked questionsMonitor budget and scope of work for contracted DM services; collaborate with study team and vendors to review DM out of scope costsOversee the tracking of Data Management timelines, ensuring that all applicable stakeholders are aware and on target for deliverables, including EDC go-live, mid-study system updates, interim data snapshots, and database locksIdentify and escalate project and quality issues; supports corrective/preventive actions as requiredSupport study-specific quality audits and regulatory authority inspections, acting as a SMEAssist in training and mentoring of other Clinical Operations personnel, providing leadership oversight and motivationParticipate in the implementation of departmental Objectives and Key Results (OKRs); recommend process improvements and initiatives to enhance operationsOther related duties, as assignedQUALIFICATIONS/KNOWLEDGE:Bachelor's degree from an accredited college or university, or equivalent work experience, preferably in a related field (Life Science/Computer Science/Statistics), requiredMinimum of 10 years relevant experience in clinical research Data ManagementSolid tumor oncology experience requiredGlobal trial experience requiredKnowledge:Working knowledge of the pharmaceutical/device commercialization process, applicable standards, and regulatory guidelines (ISO, ICH-GCP, MDR etc.)Expert understanding of global data operations tasks, specifically within Data Management and database programming and relevant data standardsDemonstrated technical experience with EDC and other data systems, preferably Medidata systemsExpert understanding of relational databases and data capture standards (e.g. CDASH)Advanced computer skills, including proficiency in MS Office (Word, PowerPoint, Outlook, Excel); including with complex pivot tables and data analysisStrong ability to identify and resolve complex challenges using critical thinking skillsExcellent organizational and record-keeping skills with strong attention to detail, precision, and accuracyAdvanced ability to manage and prioritize multiple tasks simultaneously, proactively problem-solve, and manage competing priorities and deadlinesDemonstrated ability to work well in a team as well as independently with limited oversight; is self-motivated and results-drivenExcellent verbal and written communication skills, providing clear, concise, timely, and relevant informationAdvanced vendor and relationship management skills (i.e. CROs, central laboratories, other contractors)Demonstrated ability to analyze related budgets and assess Data Management costsOTHER:Ability to lift up to 20 pounds (9 kg)Ability to travel up to 20%, both domestically and internationallyFluent in English; excellent English verbal and written communication skillsABOUT NOVOCURE:Our visionPatient-forward: aspiring to make a difference in cancer.Our patient-forward missionTogether with our patients, we strive to extend survival in some of the most aggressive forms of cancer by developing and commercializing our innovative therapy.

#J-18808-Ljbffr