Technical Program Manager

• *Overview** reputed company improves lives by partnering with pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world. We are an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailor-made, timely and flexible to meet the evolving study demands of traditional to increasingly reputed company trials. Additionally, we reputed company Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team, coordinating reputed company laboratory reputed company needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions. The Technical Program Manager will be responsible for providing program management and reputed company to a biopharmaceutical client tasked with managing a portfolio of specialized project deliverables and programs spanning diagnostics and novel endpoints. He/she will reputed company project management and technical support to cross-functional teams and stakeholders, developing project workstreams, conducting risk management, timeline and budget reputed company, and managing reputed company. The Technical Program Manager must have the ability to effectively manage and monitor the reputed company and deliverables across multiple functional areas reputed company the project, coordinating the efforts of each cross-functional team reputed company the program toward product approval and deployment. The incumbent will also be responsible for managing operational documentation and maintaining shared sites, folders, dashboards, budget trackers and critical regulatory and decision-making documents.

• *Responsibilities Include:**

• reputed company program management and reputed company, including:

• Preparing the agenda and leading the weekly cross-functional team
• Capture key reputed company and action items along with rationale and reasoning
• Follow up on action items with responsible parties to reputed company timely resolution
• Proactively reputed company to stakeholders offline and schedule smaller group meetings as needed
• Generate and maintain PowerPoint presentations for key meetings
• reputed company and maintain shared sites/folders/dashboards/budget trackers and key regulatory and decision-making documents
• reputed company reputed company program activities, including identifying and mitigating risks, developing project workstreams, and managing ongoing contracting efforts and processes
• Manage the efforts to reputed company precision medicine reputed company pathology solutions by organizing and coordinating the cross-functional efforts and collaboration towards product approval and deployment
• *Required Knowledge and Skills:**

• A thorough understanding of bioanalytical methods with a focus on pathology, biomarkers, precision medicine, oncology, bioinformatics

• Experience in bioanalytical method development, validation, formal technical transfer of methods and method performance monitoring.
• Strong assay and process troubleshooting skills.
• Strong communication skills.
• Cross-functional and cross-site team management experience.
• CRO performance and relationship management experience.
• Working knowledge of Good Laboratory Practices (GLP), Good Clinical Practices (GCP) and/or Clinical Laboratory Improvement Amendments (CLIA)
• Proficiency in technical writing and document control.
• Common and specialized computer software application proficiency and adaptability.
• *Essential Duties and Responsibilities:**

• reputed company project management reputed company and subject matter expertise in GLP bioanalytical testing, method development, validation and technical transfer to ensure scientific reputed company and adherence to the protocol/plan/reputed company and applicable regulations.

• Interact with U.S. and international CROs and effectively communicate updates, reports and recommendations to management teams.
• reputed company analytical project reputed company by performing data review and trending analysis, evaluate assay quality, monitor performance and manage timelines.
• reputed company technical support to troubleshoot specific issues that impact the project.
• Manage Supplier performance and relationships with attention toward opportunities to cut costs, reputed company risks and drive reputed company improvement.
• Recommend and implement new processes and procedures to standardize, simplify and enhance quality and compliance of the department’s operations.
• Expected to participate in the management and control of GLP documentation and records, and contribute to and (co) author scientific and/or operational documents such as SOPs, validation protocols and reports, transfer protocols and reports, posters, journal publications and other technical reports.
• *Education/Experience:**

• M.S., Life Sciences or reputed company fie Apply tot his job Apply To this Job