Associate Director - Clinical Operations

Piper Companies is seeking an Associate Director of Clinical Operations (Hybrid) to join a clinical research organization in Bethesda, MD. The Associate Director of Clinical Operations (Hybrid) will provide oversight of clinical operation activities. Responsibilities of the Associate Director of Clinical Operations (Hybrid) : Oversee clinical operations activities, including project management, site management, and clinical systems management Utilize data analytics and risk-based quality management monitoring Support government or commercial contracts in various therapeutic areas such as infectious disease, oncology, and medical devices Manage project deliverables within budget and timelines across multiple functional areas Provide operational expertise and support for clinical trial activities and strategy Requirements for the Associate Director of Clinical Operations (Hybrid) : Minimum 10 years of experience in the pharmaceutical or biotechnology industry, including at least 6 years in project management or clinical trials and operations management Centralized monitoring experience Bachelor's or Master's degree preferred Compensation for the Associate Director of Clinical Operations (Hybrid) : Salary Range: $135,000 - $175,000 depending on experience Comprehensive Benefits : Medical, Dental, Vision, 401k, Hybrid , PTO, Sick Leave as required by law, and Holidays Keywords: CRO, contract research organization, clinical trials, clinical operations, associate director, director, senior manager, manager, centralized monitoring, pharmaceutical, biotechnology, project management, site management, clinical systems management, data analytics, risk based quality management monitoring, infectious diseases, oncology, medical device, remote oversight, regulatory documents, site monitoring, GCP, ICH, data management, data analysis, project management, project management oversight, Quality Management System, risk-based quality content reviews, monitor internal/external KPIs, clinical research, clinical trial monitoring, clinical study design, RBQM, RBM, centralized data, infrastructure, risk based management, central risk, dashboard #LI-HYBRID #LI-JA2 This job opens for applications on February 28, 2025. Applications for this job will be accepted for at least 30 days from the posting date.

Created: 2025-03-10