Cam Thompson Email & Phone Number

United States

•Work as a cross-functional project manager in a diverse, fast-pace and ever changing environment; Oversee the full integration of 15-30 multi-center phase I-IV clinical trials from startup to closeout activities across the globe and different therapeutic areas. Projects have increasing complexity and contracts ranging from 65k to 260k.•Facilitate interaction with clinical teams, functional leads, and stakeholders to drive project timelines, manage budgets, mitigate risks, and ensure all deliverables meet/exceed Client’s expectations, thus gaining repeat Clientele. •Generate and manage study documents following protocol, GCP/ICH, and FDA guidelines. Example docs include MSAs and Contracts, Change Orders, Billing Invoices, Maintenance trackers, Study Plans, Approval and Change Logs, Closeout files and Work Instructions.•Proficient use of Project Management tools for tracking and reporting, such as EDCs and DBMS, Google Docs, Jira, MS Office Suites (Project/Lists/Outlook), SharePoint, and Spreadsheets.

•Draft instructional guidelines, lesson plans, learning reinforcement tools, and track training certifications.

Indianapolis, Indiana, United States

•Facilitate smooth transition from interviewing, to initial onboarding, to full team integration for new staff.•Oversee cross-functional training, mentoring, and monitoring of assigned tasks and performance metrics.•Generate complex metric reports by pulling from multiple source files for Sponsor and senior leadership, including QC reports, internal audit preparation, and team performance review using: Adobe, Basecamp/Google Docs, Greenphire, EDC and other DBMS, Jira, MS Office Suites (Project/Teams/Outlook/pptx), and Spreadsheets.•Create and maintain study documents per GCP/ICH, FDA, and University guidelines.•Manage policies, SOPs, presentations, and training material to enhance team deliverables and ensure consistency in exceeding study deliverables: 66% recruitment and screening rate, 91% longitudinal clinic enrollment retention rate, 93% participant compliance rate, and overall exceptionally high Client and Patient satisfaction. •Field questions from senior leadership, Sponsor, global research centers, and CRO/TPO and inform all parties of important timelines, risks, and AEs, as well as resolutions.•Track study payment, other stipends, travel reimbursement, inventory, shipping, and study expenses.•Oversee startup and closeout of multiple pilot studies, including preparation of monitoring reports, investigator close out reports, and investigational device accountability reports for TPOs.•Organize annual department wide educational symposium and monthly team building events.•Certified Clinical Research Professional (CCRP)- SOCRA, Aug 2018–Present.•Completed leadership training courses, Intergroup Dialogue Training and Leading IU Series, 2021–2022•Recipient of Dept. Research Staff Recognition Award for excellent study leadership & enormous individual contributions.

Indianapolis, Indiana, United States

•Prepare budget reports for study leadership and interface directly with couriers and TPOs.•Manage high volume of participant screening and scheduling calls for genetic counseling to review results.•Organize all testing kits, perform routine quality audits, and prepare completed lab reports.•Partner with global investigator sites for longitudinal enrollment of subjects with rare Parkinson’s variants.•Coordinate Outlook calendars, train staff, and maintain meticulous study records across UIs and DBs.•Accession I.U. Genetics Biobank bio-specimens for large multi-site clinical studies via OnCore.

6701 Hoover Rd, Indianapolis, In 46260

•Train and supervise instructors, mentor seasonal camp staff, and oversee both junior and adult clinics, private lessons, and special program event planning.•Draft instructional guidelines, lesson plans, learning reinforcement tools, and track staff certifications.•Perform monthly inventory of program supplies and resale to proactively reorder program equipment.

Indianapolis, Indiana, United States

•Manage processing, routing, and QC audits of irreplaceable specimens in a fast-paced high-volume lab.•Awarded 9 consecutive month bonuses for excellence in quality, efficiency, and training as team lead.

Indianapolis, Indiana, United States

•Aggregate and present findings on student-patient encounters of metabolic conditions using PeopleSoft, Access, & SPSS.

•Plan, execute, and present findings on subclinical delusion ideation studies using Excel, SPSS, and PPTX.

Master Of Public Health (Mph), Epidemiology

•As a Graduate Research Assistance, aggregate and present findings on student-patient encounters of metabolic conditions using PeopleSoft.

Bachelor Of Arts - Ba, Psychology

Activities and Societies: Women's Tennis Scholarship (4 years) | Student-Athlete Advisor Committee (SAAC) | Community Volunteering |.