Senior Director - Real World Evidence

October 2

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Clinical Outcomes Solutions

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Patient Reported Outcomes • Health Economics and Outcomes Research • Clinical and Observational Research Design and Execution • Outcomes Regulatory Support • Statistics and Psychometrics

51 - 200

Description

• Act as senior scientific oversight in RWE projects using retrospective or prospective data. • Lead growth in collaboration with subject matter experts and business developers. • Serve as thought leader and subject matter expert in real-world evidence. • Assume overall responsibility for team or area of responsibility, providing vision and leadership. • Provide oversight and direction to employees in accordance with company policies and procedures. • Lead employees to meet the organization's expectations. • Solve complex client issues in a timely and appropriate manner. • Responsible for operational responsibilities and activities of the department. • Plan and allocate resources to effectively staff and accomplish the work. • Identify opportunities to improve efficiency of business processes and procedures. • Foster a spirit of teamwork and unity among the team. • Build, manage, and mentor a strong, proactive team. • Develop, evaluate and validate tools to efficiently meet project needs. • Occasional travel required.

Requirements

• Master’s or PhD degree in Epidemiology, Public Health, Biostatistics, Data Science, or relevant scientific field. MBA, MD or PhD highly desirable. • 10+ years’ experience at a minimum in consulting, clinical trials or health research environment. Previous people management experience required (5+ years). • Proven record of leading a variety of RWE studies (retrospective and/or non-interventional prospective studies) and experience with advanced epidemiological methods (e.g. target trial emulation). • Excellent knowledge of US RWD sources (e.g. contents, quality, process to data access) including administrative claims, electronic health record databases, registries and ability to make recommendations on fitness for purpose for specific RWE studies. Knowledge of non-US databases would be a plus. • Thorough understanding of formal guidance on RWE methods by regulatory and reimbursement bodies and trending methodologies. • Proven management skills with the ability to build, train, mentor and motivate a team. • Thorough understanding of financial reporting, general project management, and accounting principles. • Thorough understanding of the biopharmaceutical R&D process in combination with solid business acumen and an appreciation of the broader business issues. Excellent interpersonal, verbal and written communication skills. • Excellent critical thinking and problem-solving skills. • Influencing skills. • Ability to manage multiple and varied tasks and prioritize workload with attention to detail. • Financial and business acumen.