CLINICAL RESEARCH COORDINATOR I (3)

University of Alabama at Birmingham; University (FL); On-site; USD 43,890 - 71,320; Full time

Job summary

The University of Alabama at Birmingham is seeking a Clinical Research Coordinator I to provide support in studies at the O'Neal Comprehensive Cancer Center. This role involves managing data collection, recruitment, and participant follow-up.

Qualified candidates should have a High School diploma or GED, with a preference for a Bachelor's in a related field. The salary range for this position is between $43,890 and $71,320 annually, with an onsite work arrangement.

Qualifications

• High School diploma or GED required.
• Bachelor's degree preferred with two years of related experience.
• Knowledge of clinical trial processes and data collection.

Responsibilities

• Serve as coordinator for clinical studies and ensure compliance.
• Collect and document data for research programs.
• Assist in recruiting and following up with research participants.

Skills

Knowledge of medical terminology

Data entry skills

Communication skills

Education

High School diploma or GED

Bachelor's in Biomedical Science, Biology, or Chemistry

Tools

Electronic Data Capture (EDC) systems

Microsoft Office products

Job description

CLINICAL RESEARCH COORDINATOR I (T235919)

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 the Deep South region. Leading-edge treatments or clinical trials can benefit patients who may not otherwise have access at local community hospitals or smaller cancer centers. The center powers more than 400 scientists and physician-scientists, cares for 20,000 patients annually, and employs over 160 staff members, along with physicians and clinical staff engaged in cancer patient care.

https://www.uab.edu/onealcancercenter/

Please attach a current resume with this application.

General Responsibilities

• Serve as coordinator for studies and provide support to other team members within the confines of the protocol as directed.
• Support screening and participant eligibility determination, working with senior team members to ensure compliance.
• Conduct activities in accordance with the protocol, regulations, and Good Clinical Practice (GCP).
• Assist with the study life cycle from start-up to closure, including collecting and recording data, recruiting and performing follow-up with participants, scheduling visits, and coordinating lab and fieldwork.

Key Duties & Responsibilities

1. Collect and document data for clinical research programs, recruit and perform follow-up with research participants, and schedule visits according to research protocols.
2. Assist in coordinating lab and fieldwork, scheduling additional procedures as necessary, preparing for and participating in study monitoring visits, and assisting with correcting findings.
3. Participate in study meetings and conference calls.
4. Assist with the completion of Case Report Forms (CRF) according to protocol.
5. Assist with development of protocols and standard operating procedures (SOPs) for data.
6. Perform administrative duties in support of research conduction as needed.
7. Prepare source documentation for review with investigators.
8. Assist in compiling, editing, and proofreading written reports for internal and external offices.
9. Use Electronic Data Capture (EDC) systems under supervision.
10. Perform other duties as assigned.

Annual Salary Range

$43,890 - $71,320

Qualifications

High School diploma or GED required.

Preferences

• Bachelor's in Biomedical Science, Biology, or Chemistry and two (2) years of hands‑on interaction, assessment, and treatment of patients, commonly found in hospitals and clinics.
• Knowledge of medical terminology, medical technology, and electronic data capture experience.
• Knowledge of clinical trial processes, data collection, and data entry.
• Experience with recruiting and performing follow-up with research participants as protocols outline.
• Knowledge of protocols and SOPs for data quality assurance.
• Must be able to walk 1.5 miles/day and lift 15 lbs.
• Knowledge of Microsoft Office products.
• Written and verbal communication skills.
• Data entry skills.

UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.

Primary Location

University

Job Category

Clinical Research

Organization

310008400 Comprehensive Cancer Center

Employee Status

Regular

Shift

Day/1st Shift

Work Arrangement

Onsite