CLINICAL RESEARCH COORDINATOR I
University of Alabama at BirminghamJobsCloseBy Editorial Insights
University of Alabama at Birmingham's Clinical Research Coordinator I is an entry-level role that supports the full clinical trial lifecycle under experienced investigators, coordinating day-to-day study activities while ensuring compliance with protocols, federal regulations, and Good Clinical Practice. You’ll assist with start-up, screening, consent, visits, data collection, and study closeout in a collaborative, hybrid, day-shift environment. The ideal candidate has a high school diploma or GED, strong Microsoft Office and data-entry skills, and excellent written and verbal communication. Salary ranges from $43,890 to $71,320. To apply, tailor your resume to show start-up through closeout experience, regulatory exposure, data integrity, and teamwork, and highlight readiness for hybrid work and the UAB location.
Description
The University of Alabama at Birmingham (UAB), Neurosurg-Clinical Research, is seeking a Clinical Research Coordinator I.
The Clinical Research Coordinator I supports the successful execution of clinical research studies by coordinating day-to-day study activities in accordance with study protocols, federal regulations, institutional policies, and Good Clinical Practice (GCP) guidelines. Under the guidance of senior research staff and investigators, this role assists with all phases of the clinical trial lifecycle, including study start-up, participant recruitment and screening, data collection, study visits, regulatory compliance, and study closeout. The Clinical Research Coordinator I works collaboratively with investigators, research teams, and study participants to ensure high-quality research operations while maintaining compliance with applicable regulatory and ethical standards. Get informed consent and answer questions related to the study with help from the Principal Investigator. Study visits, scheduling, and data tracking.
General Responsibilities
To serve as coordinator for studies and provide support to other team members within the confines of the protocol as directed.
To support screening and participant eligibility determination, working with more senior team members to ensure compliance.
To conduct activities in accordance with the protocol, regulations and Good Clinical Practice (GCP).
To assist with the study life cycle from start-up to closure, i.e., collecting and recording data, recruiting and performing follow-up with participants, scheduling visits and assisting in coordination of lab and fieldwork.
Performs other duties as assigned.
Annual Salary Range: $43,890 - $71,320
Qualifications
High School diploma or GED required.
Preferences
Ability to operate various office equipment, including printers, computers, and various software packages.
Interpersonal skills.
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.