Senior Clinical Policy Research Professional
HumanaFull Time
Senior (5 to 8 years)
Candidates should possess a Bachelor's or advanced degree in Life Sciences, Nursing, Pharmacy, or a related field, with 5-7 years of total experience. This includes 3+ years of hands-on experience in clinical operations or program management, ideally within mental health, biotech, or pharma. A solid understanding of the clinical trial lifecycle, GCP, and FDA/EMA regulations is necessary, along with a proven ability to manage multiple concurrent studies with cross-functional teams and exceptional organizational, communication, and stakeholder-management skills.
The Senior Research Program Manager will manage clinical study activities from protocol initiation through close-out, ensuring adherence to timelines, quality, and compliance. Responsibilities include developing and maintaining detailed project plans, timelines, and budgets, tracking study progress against milestones, and proactively identifying and mitigating risks. The role involves coordinating cross-functional timelines for on-time, within-budget execution, overseeing protocol adherence and compliance including IRB submissions and financial tracking, and managing study protocols in alignment with GCP and regulatory standards. Daily reviews of quality and study-related records, initiating internal audits, identifying nonconformances, and ensuring corrective actions to maintain data integrity are also key duties.
Personalized mental health solutions for employers
Spring Health offers personalized mental health solutions to employers and health plans, focusing on enhancing employee well-being. Their Precision Mental Healthcare system tailors support to individuals, providing options like digital resources, therapy, and medication. Users receive a customized care plan after a brief assessment, allowing them to schedule appointments and access wellness exercises easily. The goal is to improve workplace mental health by providing effective and accessible resources.