Senior Project Manager

Bachelor's degree, preferably in life science area or public health. 5 years working in the clinical trials/research industry. At least 2 years leading and managing full-service research studies. Experience working with observational or low-interventional research studies. Experience leading complex real-world or clinical research studies using structured project management methodologies (PMP or equivalent). Direct experience with medical records and claims data in the biopharmaceutical or RWD industry. Strong history of driving outcomes across multidisciplinary teams. Excellent communication, collaboration, and interpersonal skills. Solutions-driven mindset with the ability to anticipate blockers, manage ambiguity, and keep projects on track. Meticulous attention to detail and a commitment to quality. Well-versed in relevant research regulations (e.g., ICH-GCP, HIPAA). Comfort working in a tech-enabled or AI-enhanced environment.

Provide functional leadership and drive end-to-end study execution. Drive cross-functional execution by anticipating needs and risks. Implement clear and scalable project governance practices. Act as the financial steward of studies, managing forecasting, reporting, and scope changes. Champion the adoption of AI-enabled tools. Own the flow of study-critical information. Ensure successful and timely execution of study designs, patient recruitment, data collection, and analytics. Monitor project progress, identify risks, and implement corrective actions. Manage external vendor workstreams. Inform and influence scaling of the tech-forward platform.