Summary
Overview
Work History
Education
Skills
Timeline
Generic

Frederick Betts

Joliet,IL

Summary

Experienced with coordinating research studies and managing project timelines. Utilizes organizational skills and attention to detail to ensure accuracy and compliance. Knowledge of data collection methodologies and participant engagement strategies.

Overview

10
10
years of professional experience

Work History

Oncology Research Coordinator

Advocate South Suburban Hospital
08.2024 - Current
  • Coordinates oncology trials focusing on subject screening, enrollment, and monitoring of patients
  • Advises physicians and team members associated with current status subjects
  • Accurately capturing clinical data via eCRFs
  • Maintaining source documentation
  • Closely follows subjects to report adverse/serious adverse events
  • Scheduling subjects within appropriate time windows

Clinical Research Coordinator

Hope & Healing Cancer Services
06.2024 - 08.2024
  • Regularly interfaced with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocol
  • Functioned as participants’ primary point of contact, keeping them informed on the study progress and facilitate involvement of other study team members as needed
  • Managed participant visit scheduling and technical troubleshooting, escalating issues to the appropriate individual

Clinical Research Coordinator

Intelligo Health Research
09.2022 - 03.2024
  • Central point of contact for clinical site regarding study activities
  • Consistently used study protocol and appropriate addendums for guidance
  • Diligently screened, recruited and enrolled research subjects
  • Administered informed consent process to prospective subjects
  • Directly interacted with participating subjects to collect medical history
  • Performed data entry and query resolution on Intelligo EDC platform
  • Accurately collected and shipped laboratory specimens
  • Administrated stipend payments to subjects
  • Acquired Regulatory documents from onsite personnel periodically/monthly
  • Traveled monthly to Minnesota Elligo site for enrollments and other site activities
  • Ensured the accuracy of reconciled entries during close out procedures
  • Continued in required periodic research training

Operations Specialist

MultiPlan, Inc.
05.2022 - 08.2022
  • Obtained daily mail and imaging for source documentation
  • Reviewed claims and questionnaires
  • Uploaded documents into database for end users

Clinical Research Coordinator

Spectraforce
07.2021 - 04.2022
  • Company Overview: Remote Contractor for IQVIA
  • Provided AstraZeneca Covid-19 clinical research support to virtual investigators and their study staff to prepare for and execute assigned research studies, including reviewing study protocols, associated study files, and electronic systems used to carry out the virtual clinical research study
  • Collected, tracked and submitted regulatory/ethics documentation as required by the FDA and other regulatory/ethics bodies governing the conduct of clinical research
  • Set up and maintained clinical trial filing system (electronic and paper based) to ensure accuracy and regulatory compliance
  • Supported the virtual sites with documentation preparation, completion, tracking and maintenance, Performed periodic review of regulatory site records for completeness and accuracy
  • Collected, recorded and assigned research patient calls/queries/safety reporting to appropriate team members for follow-up
  • Supported other job-related duties as assigned by the Clinical Lead
  • Remote Contractor for IQVIA

Clinical Research Coordinator

Joule Clinical Staffing
01.2021 - 05.2021
  • Company Overview: Remote Contractor for Sarah Cannon Cancer Institute
  • Part of coordinating team which oversaw data management portion of the Janssen (Johnson & Johnson) Covid-19 clinical study
  • Reviewed subject eDiary entries, searched for reactogenicity symptoms, and recorded all adverse events into Medidata Rave EDC
  • Recorded subject Visit Day occurrences with accurate details
  • Verified subject entries with offsite Data Manager to maintain Medidata Rave EDC accuracy
  • Used Clinical Conductor to authorize stipend payments and record subject Visit Days
  • Confirmed subject Study Drug Injection details in Medidata Rave
  • Verified subject post vaccination observations in Rave EDC
  • Acted to unblind/withdraw subjects from study by updating Rave EDC and IQVIA Study Hub
  • Called subjects to set appointments
  • Remote Contractor for Sarah Cannon Cancer Institute

Research Assistant

Research by Design
11.2019 - 03.2020
  • Observed and recorded clotting scores and bleeding assessments on kidney disease patients
  • Requested blood draws from dialysis technicians regarding study patients
  • Processed and packaged laboratory specimens
  • Entered patient data into Clinical Conductor electronic tracking system
  • Assisted with filing of regulatory documents
  • Assisted Study Coordinators with data entry and query resolution

Research Assistant

Northwestern University
09.2019 - 11.2019
  • Obtained participant physical measurements for 'All of Us' study
  • Collected blood pressure/pulse rate readings and urinalysis from study participants
  • Entered information of each participant into a databank
  • Recruited potential study participants via phone to schedule study appointments

Clinical Research Coordinator

Chicago Clinical Trials
06.2016 - 10.2017
  • Managed pre-study assessments regarding the start of all studies
  • Uploaded regulatory documentation to Trial Master File
  • Organized documentation for pre-study monitor visits

Analyst Clinical Services

Spectraforce
09.2015 - 12.2015
  • Company Overview: Contractor for CVS Health
  • Supported the communication campaign for CVS Health by generating mailing lists based on recent prescription claim data
  • Responsible for executing data pulls and mail merges for mandatory mailings to help consumers understand their prescription benefit changes
  • This allowed the consumer to make the appropriate changes to their medical benefit plan
  • Contractor for CVS Health

Data Analyst

Aerotek Staffing
12.2014 - 04.2015
  • Company Overview: Contractor for Baxter Healthcare
  • Generated complete and accurate reports for internal Pharmacovigilance analysis
  • Ensured that all data reports were completed and distributed to end users in a timely fashion
  • Contractor for Baxter Healthcare

Education

Master of Health Administration -

University of Phoenix
Phoenix, AZ
06.2008

Skills

  • Data management
  • EDC Medidata Rave
  • Oracle database
  • Epic software
  • Cerner software
  • MS Word
  • MS Excel
  • MS Teams
  • OneDrive
  • Meditech
  • Decentralized clinical trials
  • Medrio software
  • IQVIA Study Hub
  • ECRF query resolution
  • Clinical Conductor
  • Data analysis
  • Oral communication
  • Written communication
  • Character qualities
  • Sense of humor
  • Electronic data capture
  • Data organization
  • Microsoft office
  • Data collection
  • Planning and coordination
  • Team collaboration and leadership
  • Data entry
  • Documentation and reporting
  • Data cleaning
  • Documentation skills

Timeline

Oncology Research Coordinator

Advocate South Suburban Hospital
08.2024 - Current

Clinical Research Coordinator

Hope & Healing Cancer Services
06.2024 - 08.2024

Clinical Research Coordinator

Intelligo Health Research
09.2022 - 03.2024

Operations Specialist

MultiPlan, Inc.
05.2022 - 08.2022

Clinical Research Coordinator

Spectraforce
07.2021 - 04.2022

Clinical Research Coordinator

Joule Clinical Staffing
01.2021 - 05.2021

Research Assistant

Research by Design
11.2019 - 03.2020

Research Assistant

Northwestern University
09.2019 - 11.2019

Clinical Research Coordinator

Chicago Clinical Trials
06.2016 - 10.2017

Analyst Clinical Services

Spectraforce
09.2015 - 12.2015

Data Analyst

Aerotek Staffing
12.2014 - 04.2015

Master of Health Administration -

University of Phoenix
Frederick Betts