CLINICAL RESEARCH COORDINATOR II

University of Alabama at Birmingham; Birmingham (AL); Hybrid; USD 50,000 - 82,000; Full time

Job summary

The University of Alabama at Birmingham is inviting applications for a Clinical Research Coordinator II. This role involves coordinating clinical research studies, focusing on participant recruitment, data management, and ensuring compliance with protocols. Ideal candidates have a Bachelor’s degree and relevant clinical research experience, contributing significantly to the UAB STD Program's objectives.

Qualifications

• Bachelor's degree in a related field required.
• Three years of related experience.
• Work experience may substitute for education requirement.

Responsibilities

• Coordinate clinical research studies within the UAB STD Program.
• Responsible for participant recruitment, data collection, and maintaining study records.
• Assist with IRB submissions and regulatory binder maintenance.

Skills

Clinical research experience

Organizational skills

Education

Bachelor's degree in a related field

Job description

Join to apply for the CLINICAL RESEARCH COORDINATOR II role at University of Alabama at Birmingham

3 days ago Be among the first 25 applicants

Join to apply for the CLINICAL RESEARCH COORDINATOR II role at University of Alabama at Birmingham

The University of Alabama at Birmingham (UAB), Med - Infectious Diseases, is seeking a Clinical Research Coordinator II. Working independently under the site Principal Investigator, the Clinical Research Coordinator II will be responsible for coordinating clinical research studies within the UAB STD Program, including but not limited to participant recruitment and enrollment, study procedures, data collection, data verification, assisting with IRB submissions, and maintaining study records.

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

• Assists 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 the coordination of lab and fieldwork.
• Serves as primary coordinator for studies and provides support to other team members within the confines of the protocol as directed.
• Prepares and maintains regulatory binders for all studies.
• Documents Adverse Events (AEs) and Serious Adverse Events (SAEs) as required by protocol and regulatory guidance.
• Completes and submits expedited SAE reports per protocol.
• Follows detailed SOPs for data collection and equipment use; trains others to do the same.
• Ensures study documentation is complete and compliant with study protocols.
• Oversees task assignments and ensures timely completion of responsibilities.
• Coordinates with departmental and financial teams for ordering, inventory management, patient payments, and budget development.
• Ensures accurate and timely data entry, collection, and reporting.
• Works with other research sites to ensure consistency across the study.
• Performs other duties as assigned.
  
  

Annual Salary Range: $50,050 - $81,330

Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement.

Preferences

• Clinical research experience.
• Familiarity with UAB IRB Study Coordinator experience.
• Comprehensive understanding of related scientific and clinical terminology.
• Organizational skills.
• Understanding of research terminology.
  
  

Primary Location

University

Job Category

Clinical Research

Organization

311402400 Med - Infectious Diseases

Employee Status

Regular

Shift

Day/1st Shift

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

Remote/Hybrid Eligible

Equal Opportunity Statement

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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Higher Education

Referrals increase your chances of interviewing at University of Alabama at Birmingham by 2x

Get notified about new Clinical Research Coordinator jobs in Greater Birmingham, Alabama Area.

Community Science & Research Coordinator

Birmingham, AL $42,500.00-$45,000.00 1 week ago

CLINICAL RESEARCH REGULATORY COORDINATOR II

Behavioral Health Clinical Care Coordinator - Substance Abuse Center

Behavioral Health Clinical Care Coordinator - Substance Abuse Center

CLINICAL RESEARCH REGULATORY COORDINATOR III

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.