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CLINICAL RESEARCH COORDINATOR I (6)

University of Alabama at Birmingham

University of Alabama at Birmingham

university, fl, usa
Posted on Friday, April 26, 2024
CLINICAL RESEARCH COORDINATOR I (6) - (T216493)

Description

The University of Alabama at Birmingham (UAB), O'Neal Comprehensive Cancer Center is seeking a Clinical Research Coordinator I.

The O'Neal Comprehensive Cancer Center is one of 51 NCI-designated comprehensive cancer centers in the United States and is the only one in Alabama and in the Deep South region. A comprehensive designation also means UAB Medicine patients have access to leading-edge treatments or clinical trials that they may not otherwise have at local community hospitals or smaller cancer centers. For many, an NCI designation can hold the key to survival. On campus and around Birmingham, the O'Neal Cancer Center is a significant part of our economic powerhouse. The O'Neal Cancer Center powers more than 400 scientists and physician-scientists, cares for 20,000 patients annually, and is home to more than 160 employees, plus all the physicians and clinical staff engaged in cancer patient care. The link to our website is: https://www.uab.edu/onealcancercenter/

Please attach a current resume with this application.

General Responsibilities

  • To collect and record preliminary data for clinical research programs.
  • To recruit and perform follow-up with research participants as protocols outline.
  • To schedule visits according to research protocols.
  • To assist in coordination of lab and fieldwork.
  • To maintain familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulations.

Key Duties & Responsibilities

  1. Prepares for study monitoring visits.
  2. Assists with correcting findings.
  3. Assists with the completion of Case Report Forms (CRF) according to protocol.
  4. Assists with the development of protocols and standard operating procedures (SOPs) for data quality assurance.
  5. Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials).
  6. May perform a variety of medical procedures under supervision.
  7. May assist in compiling, editing, and proofing written reports for both internal and external administrative offices.
  8. May perform data analysis using a variety of software packages.
  9. Uses Electronic Data Capture (EDC) systems necessary for operations under supervision.
  10. Must be able to walk 1 - 1.5 mile/day. Able to bend, stand and lift up to10 lbs
  11. Performs other duties as assigned.

Annual Salary Range: $41,175 - $66,915

Qualifications

High School diploma or GED required.

Preferences

  • Bachelor's and two (2) years of experience working in a clinical setting is preferred.
  • Knowledge of clinical trial processes, data collection, and data entry.
  • Knowledge of medical terminology.
  • Experience with recruiting and performing follow-up with research participants as protocols outline.
  • Knowledge of protocols and standard operating procedures (SOPs) for data quality assurance.

Primary Location

: University

Job Category

: Clinical Research

Organization

: 310008400 Comprehensive Cancer Center

Employee Status

: Regular
Shift: Day/1st Shift
Work Arrangement (final schedule to be determined by the department/hiring manager): Onsite