Clinical Research Coordinator I
CLINICAL RESEARCH COORDINATOR I (8) - (T213652)
Description
The University of Alabama at Birmingham, 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. The link to our website is https://www.uab.edu/onealcancercenter/.
Ideal candidates must be able to walk one to one and a half (1-1.5) mile/day, and be able to bend, stand and lift up to ten (10) lbs.
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
- Collects and records preliminary data for clinical research programs. Recruits and performs follow-up with research participants as protocols outline. Schedules visits according to research protocols.
- Assists in coordination of lab and fieldwork. Prepares for study monitoring visits. Assists with correcting findings.
- Assists with the completion of Case Report Forms (CRF) according to protocol.
- Assists with development of protocols and standard operating procedures (SOPs) for data quality assurance.
- Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials).
- May perform a variety of medical procedures under supervision.
- May assist in compiling, editing, and proofing written reports for both internal and external administrative offices. May perform data analysis using a variety of software packages.
- Uses Electronic Data Capture (EDC) systems necessary for operations under supervision.
- Performs other duties as assigned.
Annual Salary Range: $41,175.00 - $66,915.00
Qualifications
- High School diploma or GED required.
Preferences
- Prefer candidates with a bachelor’s and two (2) years’ experience working in a clinical setting.
- Knowledge of clinical trial processes, data collection, data entry.
- 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.
Key Skills
- Face-to-face patient communication experience.
Primary Location
: University
Job Category
: Clinical Research
Organization
: 310008400 Comprehensive Cancer Center
Employee Status
: RegularShift: Day/1st Shift