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Rosalyn Goodwin

Rosalyn Goodwin

Clinical Research Coordinator - Oncology

Talent
South ChicagoMember since June 26, 2026
OSHAClinical TrialsInsurance verificationPatient monitoringGCPClinical researchCITI TrainingEMR Systems
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OSHAClinical TrialsInsurance verificationPatient monitoringGCP

About

Healthcare professional with varied experience. I have done clinical research, recruitment and administrative duties. My goal is to broaden my knowledge and skills while growing with a stable company or organization. I am an avid listener which is the most important thing for any job in my opinion. I learn quickly and easily adapt to changes. Authorized to work in the US for any employer

Experience

Clinical Research Coordinator - Oncology - Advocate Aurora Health - Oak Lawn, IL

(2024-06)

  • Collected and recorded data accurately and promptly using electronic data capture systems or case report forms (CRFs)
  • Recruited and screened eligible participants for clinical trials, maintaining accurate records of enrollment and eligibility criteria
  • Coordinated and managed clinical research studies, ensuring adherence to protocols, regulatory requirements, and timelines
  • Scheduled study visits, procedures, and follow-up appointments with participants in accordance with study protocols
  • Coordinated with clinical research associates (CRAs) to ensure timely resolution of data queries and discrepancies

Clinical Research Coordinator (temp) - The University of Chicago - Chicago, IL

(2023-11 - 2024-03)

  • Ensured compliance with Good Clinical Practice (GCP) guidelines throughout the conduct of clinical trials
  • Provided ongoing support to investigators by addressing queries related to study procedures or participant management issues
  • Managed investigational product accountability including receipt, storage, dispensing, reconciliation, and return/destruction processes
  • Maintained comprehensive study documentation including informed consent forms, source documents, and regulatory binders
  • Collected and recorded data accurately and promptly using electronic data capture systems or case report forms (CRFs)
  • Scheduled study visits, procedures, and follow-up appointments with participants in accordance with study protocols
  • Recruited and screened eligible participants for clinical trials, maintaining accurate records of enrollment and eligibility criteria
  • Coordinated and managed clinical research studies, ensuring adherence to protocols, regulatory requirements, and timelines

Clinical Research Coordinator - Retina Consultants of America - Columbia, SC

(2021-02 - 2023-10)

  • Managed clinical trials
  • Patient recruitment, scheduling and follow-up
  • Assisted PI in procedures to ensure protocol compliance
  • Patient monitoring and observation
  • Created patient/ study binders
  • Data systems management
  • Coordinated with monitors and sponsors
  • Entered data into records and EMR systems
  • Knowledge of regulatory guidelines relating to the active trials
  • Handled queries, AE and SAE reporting if needed
  • In charge of shipments of medications to include: documentation, storage and distribution
  • Handled Patient compensation for trial participation
  • Arranged transportation for patients in clinic
  • Knowledge of FDA audit preparation
  • CITI training on all aspects of human subject trials
  • HIPPA, OSHA, IATA certification

Front Office Manager/ Optometrist Assistant - National Vision, Inc. - Columbia, SC

(2019-11 - 2021-01)

  • Handled patient scheduling
  • Created medical record charts: hard copy and EMR
  • Insurance verification, authorization and referrals
  • Performed minor repairs on glasses
  • Instructed patients on contacts application and removal
  • Patient eye exams and work-ups
  • Assisted physicians when needed
  • Ordered supplies for office
  • Scheduled front desk employees to ensure coverage
  • Shipment of glasses and contacts to customers
  • Coordinated with laboratories to expedite emergency orders

Recruiter/HR Generalist - Medical Staffing Network - Columbia, SC

(2003-05 - 2006-01)

  • Candidate sourcing for medical facilities
  • Provided medical staff for hospitals, prisons, patient sitting and home health
  • Conducted interviews, background checks and orientations
  • Handled the after hours emergency staffing
  • Handled any testing needed by the clients to access skills
  • Light payroll duties: issuing checks or payment cards
  • Coordinated background checks, reference checks, drug tests or any other pre-employment screening processes as required by company policy or client requests
  • Provided regular updates to hiring managers on recruitment progress, including candidate pipeline status reports
  • Collaborated with HR team members to develop standardized interview questions that assessed core competencies
  • Coordinated new hire orientation sessions, ensuring a smooth transition into the organization for all new employees
  • Assisted with employee onboarding activities such as completing paperwork, conducting orientations, and facilitating training sessions

Float Staff - Physicians Practice Services - Columbia, SC

(1998-01 - 2000-04)

  • Traveled to different doctor offices within the network
  • Handled patient check in/ check out
  • Insurance verification, referrals and authorizations
  • Checked vital signs
  • Collected and tested specimens ordered by the physician
  • Created medical record charts
  • Medicare/ Medicaid billing

Education

Bachelor of Science - Biology - Georgia Southern University (1992-09 - 1996-08)

Skills

Clinical Research Coordinator - Oncology

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