Bryan Bear Email & Phone Number

St. Louis, MO, US

Greater St. Louis Area

• Manage daily clinical operations for research trials
• Act as a liaison between research staff and treatment staff to streamline research visits for patients participating in clinical studies
• Work with clinical research staff by identifying risks and developing an action plan to resolve any potential issues prior to patient arrival
• Provide clinical research coordinators with support and direction
• Assist with organization, implementation, and management of complex phase I-III clinical projects for solid tumor and bone marrow transplant to ensure trials are conducted in accordance to the protocol and standard.
• Excellent ability to understand intricate protocols (e.g. treatment regimens, dose limiting toxicities, dose holding parameters, etc.)

Greater St. Louis Area

• Reviewed and presented financial disclosure statements for review by the Disclosure Review Committee (DRC) Chair
• Processed transactional disclosures of financial interest and coordinated management with various University offices
• Made initial determination of Financial Disclosure Statements to determine the nature of potential conflict of interest
• Generated official correspondence (on behalf of the DRC Chair) implementing and maintaining conflict of interest management plans
• Prepared case specific materials for DRC Subcommittee meetings
• Communicated with faculty to clarify issues of conflict and provide guidance and education on conflicts of interest

Greater St. Louis Area

• Conducted quality assurance audits of clinical studies (trial master files) to ensure trials are conducted in accordance with the protocol, any/all appropriate regulatory agencies, local and institutional requirements
• Applied clinical experience to understand intricate protocols (e.g. objectives, treatment regimens, dose limiting toxicities, dose holding parameters, etc.)
• Utilized a robust medical terminology arsenal to easily interpret doctor notes, lab results, orders, treatment records, diagnostic testing and pathology reports.
• Used strong investigative skills to identify and confirm initial and continued patient eligibility
• Employed and understood vetted resources to confirm concomitant medications are appropriate for enrollment as well as throughout trial.
• Identified and summarized protocol deviations and Serious Adverse Event occurrences

Greater St. Louis Area

• Department of Psychiatry
• Coordinated and managed research projects for the Alzheimer’s Disease Research Center and the Conte Center for Neuroscience Research
• Reviewed and cross-checked protocols with Case Report Forms for consistency within each document
• Carried out the consenting process with potential research participants
• Performed eligibility checks on potential research study participants
• Prepared amendments and continuing review applications for IRB review and approval

Greater St. Louis Area

• Acted as a liaison between physicians, nurses, accountants, and pharmacists
• Produced monthly accounting reports
• Prepared reports of antipsychotic medication usage trends to the Missouri Department of Mental Health
• Facilitated yearly inventory audit with the Missouri Department of Mental Health accounting department
• Developed and implemented new process for inventory maintenance
• Processed and delivered physician’s orders