Christopher Dosier Email & Phone Number

Chester, VA, US

Richmond, Virginia, United States

• Initiates, directs, and leads team meetings, prepare reports, maintains project schedules and plans, and drives operational readiness to ensure project deliverables are completed according to desired timelines
• Assists in the tracking of project specific budgets
• Creates and coordinates project schedules and maintaining the process for regular reviews and updates
• Conducts risk management and scenario planning as well as develops contingency and/or risk mitigation plans.
• Tracks and reports on project milestones and providing status reports to stakeholders; highlighting action items.
• Proactively identifies, communicates, and/or troubleshoots any issues or problems throughout the project life cycle

Richmond, Virginia Area

• Lead instructor for Senior and Graduate level engineering course examining commercialization of intellectual property and pathways to market with a focus on biotechnology and drug development
• In depth analysis of patents and intellectual property, start-up/small business strategy, product design and development, regulatory strategies (FDA, CMS, etc.) and frameworks, quantitative market analysis, finance and.
• Provides students with real-world product-market fit analysis techniques and product development strategies to address unmet market needs and provide functional solutions to clients
• Training students on concise presentation of market data, product positioning, proof of concept requirements, contingency planning and risk mitigation, and funding strategies
• Leads multiple student groups on project management - initiation, planning, execution, control and closure in a semester long team project leading to a novel product deliverable using MS Project

Richmond, Virginia, United States

• CRO program manager providing program leadership and directing cross-functional teams for clinical monitoring for Pre-clinical through Phase III global clinical trials
• Manages the technical performance of staff and laboratory assays according to Standard Operating Procedure (SOPs), Good Clinical Practice (GCP), Good Laboratory Practice (GLP) guidelines, ICH guidelines and other.
• Client liaison that builds and maintains client relationships and communication and adheres to project timelines, deliverables, budgets, reports, and financial targets
• Reviews clinical study protocols and manages team and functional support group resources to meet project timelines and deliverables with adherence to FDA and ICH methods and SOPs
• Accountable to 12 direct reports and 11 indirect reports across multiple client programs
• Provides real-time project status to multiple client groups and oversees project metrics and execution of project goals and milestones in weekly meetings

Richmond, Virginia, United States

Group Leader in Clinical Research Group (CRG) at Thermo Fisher Scientific. Responsibilities include project management for pharmaceutical development, coordination of sample analysis, quality control of data generated, and reporting of results to clients.

• Program manager and Principal investigator for early-stage biotechnology lab focused on stem cell, protein, and drug delivery research and development using hydrogel systems
• Identified and secured non-dilutive funding opportunities (federal and state), formulated contract budgets, project management and milestone targets, experimental research design and protocol execution; operational.
• Raised several million dollars in non-dilutive funding primarily through Department of Defense Small Business Innovative Research (SBIRs) contracts and other government contracts
• Collaborated with research universities to commercialize technologies and evaluate efficacy in clinically relevant animal models to simulate human disease states
• Established Standard Operating Procedures (SOPs) for lab operations and assay performance
• Designed and presented high quality venture capital pitch decks for funding opportunities

Richmond, Virginia

• Advising in the design of microfluidic systems to test blood fractionating technologies
• Optimizing system setup to standardize and increase the efficiency of blood separation into component parts, with a focus on the isolation of leukocytes from whole blood samples.
• Designed, performed, and analyzed data from experiments on microfluidic devices for the separation of blood cells for FDA Class II Medical diagnostic instrument development
• Prepared weekly reports and participated in planning and execution of milestones to secure investor funding and milestone payments
• Co-author on two publications for separation of T-cells from whole blood for CAR T-cell immunotherapies

• Ph.D. thesis project focused on use of multiple stem cell sources for bone tissue engineering and effective delivery of stem cells using biologically active hydrogels
• Collaborated with multiple labs and institutions and training of other researchers
• Provided quarterly updates to multiple funding institutions
• Three first author publications resulted from graduate thesis work
• Co-authored 3 additional publications and numerous conference presentations

• Ran independent experiments examining stress-strain relationships and the physiologic response to deformation in smooth muscle tissue.
• Provided data and co-authored 2 papers as an undergraduate researcher

Master Of Business Administration (M.B.A.), 4.0

Phd, Bioegnineering

Activities and Societies: BGSAC, BBUGS

Bachelor Of Science, Biomedical Engineering, 3.98

Activities and Societies: Tau Beta Pi

Bachelor Of Science (B.S.), Physics, 3.98