Michael Poschel Email & Phone Number

Acworth, Ga, Us

United States

Atlanta Metropolitan Area

Spearheaded the administration of clinical trial contracts, surpassing $15 million, across a spectrum of indications. Managed the comprehensive life cycle of 100,000+ samples, encompassing testing, analysis, and reporting.• Orchestrated and supervised planned PM activities through effective collaboration with a cross-functional team.• Spearheaded the implementation and management of both new and existing projects following Precision for Medicine's repository mission and management philosophy.• Developed and sustained logistical plans, advising clients on study designs to elevate quality and efficiency.• Created and managed multiple project timelines, budgets, revenue goals, and resource plans compared to contracted project scope(s), fully exploring innovative ideas that optimized quality and efficiency.• Managed the day-to-day coordination and supervision of scheduled activities with precision, assigning responsibilities to facilitate the completion of contracted work activities.• Developed daily professional communications and played a role in the design of new tasks and projects for internal and external stakeholders.• Achieved all revenue and gross margin targets allocated to projects, managing project expenses and client billing effectively.• Emerged as the point of contact between Precision and external clients, embodying the "face of the business." Ensured decisions aligned with the overarching goal of customer-centricity to surpass client expectations across full-service portfolios.• Ensured the alignment of work products with design and performance standards, regulatory parameters, and customer expectations, upholding and enforcing standards at every step in the project execution process.• Estimated, acquired, and allocated human and material resources, and assessed and mitigated technical, project, and business risks.

United States

Oversaw and directed clinical trials for a diverse range of organizations, including AnaptysBio, Artiva Bio, BeiGene, BioMed Valley, CareDx, Elucida Oncology Inc, Fisher Bioservices, GeneDx, Ikena Oncology, Jasper Therapeutics, Kirin Kyowa Inc, Nuvalent Inc, PACT Pharma, PATH, Patients Like Me, and St. Jude Research.• Directly supervised, managed, and ensured follow-up on assigned projects or projects delegated by direct reports.• Directed client-facing interactions while maintaining effective coordination with the technical team.• Established and maintained communication with internal and external clients, customers, team members, and various stakeholders.• Supported the senior project director in ensuring adherence to terms specified in awarded contracts during the management and execution of all projects.• Stayed up-to-date on IATA shipping regulations, consistently maintaining certification and upholding standards.• Assisted in crafting documents to ensure successful overall project delivery and internal compliance with SOPs.• Grasped the project scope, including collaborating with the primary project manager to establish and maintain project timelines, and participating in internal and client meetings with key stakeholders.• Offered meticulous daily coordination, comprehension, and supervision of scheduled activities, balancing responsibilities for contracted work and lab schedule requirements, and compiling status updates for all project deliverables. • Managed allocated projects to attain business revenue objectives, consistent with Precision for Medicine's mission and management philosophy, and ensured timely fulfillment of all requests.• Collaborated closely with project managers to conclude monthly client invoices and engage in forecasting exercises.• Offered assistance in various project financial activities requested by internal or client teams and played a role in preparing change orders for project managers and clients.

Decatur, Georgia, United States

Directed the management and execution of clinical trials for Aeon, Alzheon, AriBio, Biogen, Cortexyme, Eisai, Impax, NeuroDerm, and Sage Therapeutics.• Screened subjects and gathered pertinent data according to study protocol, performed routine maintenance visits with randomized subjects, and organized subject appointments, including MRIs and PET scans.• Captured subject data using tablets, produced printed exam results for subject binders under the coordinator's purview, and promptly addressed queries related to exams.• Utilized an electronic database tool to enter data and conducted thorough reviews of lab report results.• Collaborated with clinical research assistants to facilitate monitoring visits and participated in close-out visits.• Supported the pharmacist in compounding Investigational Product (IP) within IV bags, overseeing the temperature of both refrigerated and ambient IP through digital and manual monitoring.• Maintained daily records of Investigational Product (IP) dispensed and organized crucial documents, including temperature excursion reports and adverse events related to IP.• Oversaw the receipt of vendor Investigational Product (IP) and systematically logged the received IP into a database management system.

Marietta, Georgia

Directed account management for Allergan/Tobira, AstraZeneca, Biogen, BeiGene, Celgene, MedImmune, Merus, Pierre Fabre, Receptos, and Reistone.• Completed the finalization of lab reports for site viewing and analysis, and reconciled data collected by sponsor and Clinical Research Organization (CRO) teams with the Q2 Solutions database.• Coordinated meetings with Clinical Research Organizations (CROs) and Sponsor teams and developed study flowcharts and other instructional documents.• Managed the procurement of lab kits, both initial and resupply, and coordinated the shipment of samples from Q2 Solutions storage locations to third-party laboratories for testing.• Generated requisition forms for patient visits and addressed inquiries related to requisition forms.• Developed and executed training sessions for new project coordinators, emphasizing proficiency in Q2 Solutions systems.• Facilitated virtual meetings with Clinical Research Organizations (CROs) and sponsor teams.