CLINICAL RESEARCH COORDINATOR I

University of Alabama at Birmingham; Birmingham (AL); On-site; USD 44,000 - 71,000; Full time

Job summary

The University of Alabama at Birmingham (UAB), Psych - Behavioral Neurobiology, is seeking a Clinical Research Coordinator I.

This role supports clinical research at the intersection of infectious disease and addiction medicine, involving individuals with substance use disorders and those at risk for infectious diseases. Responsibilities include coordination of study activities, regulatory compliance, and communication across teams.

Qualifications

• High School diploma or GED required.
• Bachelor's degree in public health, biology, health sciences, psychology, social work, or a similar discipline preferred.
• The ability to learn and apply clinical research principles and regulatory requirements.
• Experience in a healthcare, research, public health, social services, or related setting preferred.
• Experience interacting with study participants and performing data collection or administrative tasks is preferred.

Responsibilities

• Recruits, screens, consents, and enrolls participants for research studies focused on infectious diseases and substance use.
• Coordinates study visits, maintains participant engagement and retention, and serves as a primary point of contact for study participants.
• Collects, enters, and manages study data.
• Maintains study records and regulatory documentation.
• Supports data quality assurance and reporting requirements for grant-funded research activities.
• Performs other duties as assigned.

Skills

Participant interaction

Education

Bachelor's degree in public health or related field

Job description

Job Description - CLINICAL RESEARCH COORDINATOR I (T239476)

CLINICAL RESEARCH COORDINATOR I - ( T239476 )

Description

The University of Alabama at Birmingham (UAB), Psych - Behavioral Neurobiology, is seeking a Clinical Research Coordinator I.

This position will support clinical research at the intersection of infectious disease and addiction medicine, primarily involving individuals with substance use disorders and those living with or at risk for infectious diseases. Studies range from observational and implementation research to clinical trials and involve recruitment, informed consent, data and specimen collection, participant follow-up, and coordination of study visits. The CRC I will work closely with investigators, clinicians, research staff, and community partners to coordinate study activities, maintain protocol and regulatory compliance, and support communication across multidisciplinary study teams.

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.

Key Duties & Responsibilities

• Recruits, screens, consents, and enrolls participants for research studies focused on infectious diseases and substance use.
• Coordinates study visits, maintains participant engagement and retention, and serves as a primary point of contact for study participants.
• Collects, enters, and manages study data.
• Maintains study records and regulatory documentation.
• Supports data quality assurance and reporting requirements for grant-funded research activities.
• Performs other duties as assigned.

Annual Salary Range: $43,890 - $71,320

Qualifications

• High School diploma or GED required.

Preferences

• Bachelor's degree in public health, biology, health sciences, psychology, social work, or a similar discipline preferred.
• The ability to learn and apply clinical research principles and regulatory requirements.
• Experience in a healthcare, research, public health, social services, or related setting.
• Experience interacting with study participants, patients, or community members and performing data collection or administrative tasks is preferred.

MVR Needed.

Equal Employment Opportunity

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

Employee Status

Regular

Shift : Day/1st Shift

Work Arrangement (final schedule to be determined by the department/hiring manager) : Onsite