CLINICAL RESEARCH COORDINATOR III

UAB group; Birmingham (AL); Hybride; USD 61 000 - 99 000; Plein temps

Résumé du poste

The University of Alabama at Birmingham (UAB), Psych - Behavioral Neurobiology, is seeking a Clinical Research Coordinator III. This role leads coordination, ensuring regulatory compliance and oversees staff while managing the lifecycle of clinical studies from start-up to close-out.

The position requires a Bachelor’s degree in a related field with 5 years of experience, with CCRP/CCRC preferred. A master’s degree is preferred and may enhance qualifications for advanced responsibilities.

Qualifications

• Bachelor's degree in a related field and five (5) years of related experience required.
• Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification preferred.

Responsabilités

• Provide oversight to less experienced staff to ensure quality and regulatory compliance with clinical research operations.
• Coordinate and manage the research study lifecycle from start-up through close-out.
• Coordinate and conduct screening, scheduling, consenting, assessing, ordering, collecting, documenting and shipping under GCP.
• Develop protocol-specific systems, documents, SOPs, training manuals and CRFs.
• Prepare study budgets and coordinate studies of various complexities.
• Interpret and apply current research findings and report at conferences/journals.
• Prepare IRB/IND/FDA submissions and educational materials.

Connaissances

Regulatory compliance

Clinical research coordination

Formation

Bachelor's degree in related field

Master’s degree in related field

Description du poste

Job Description - CLINICAL RESEARCH COORDINATOR III (T240596)

CLINICAL RESEARCH COORDINATOR III - ( T240596 )

Description

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

General Responsibilities

To serve as a lead coordinator by providing oversight to less experienced staff to ensure quality and regulatory compliance with clinical research operations.

To coordinate and manage the research study lifecycle from start-up through close-out.

To coordinate and conduct all applicable clinical and administrative activities required by the protocol such as screening, scheduling, consenting, assessing, ordering, collecting, documenting and shipping under the auspices of Good Clinical Practice (GCP).

Key Duties & Responsibilities

Manages all aspects of research program and clinical studies including education/training.

Develops protocol-specific systems and documents including process flows, training manuals, SOPs, and CRFs.

Prepares study budgets as needed.

Coordinates studies of all complexities.

Acts as a consultant within area of clinical expertise.

Provides a lead role in determining participant eligibility.

In addition to creating study documentation, may provide oversight to junior staff members as well as for items such as source, lab, and pharmacy orders, flowsheets, and adverse events.

In conjunction with PI or Director, interprets and applies current research findings in area of clinical specialty and reports findings in professional journals and local, state and national conferences.

Prepares and submits multiple levels of research documentation (i.e. IRB, IND, or FDA submissions, educational materials, reports, grant renewal reports, and study forms).

Maintains compliance with federal, state, and accrediting agencies (sponsors), including maintaining any required documentation.

Conducts literature reviews, participates in grant writing and development, and contributes to assessing solutions for operational shortcomings of data procurement in protocol design.

Participates in data analysis and research dissemination activities (e.g., conferences, peer-reviewed articles) under the direction of the PI.

Performs other duties as assigned.

Annual Salary Range

$60,835 - $98,855

Qualifications

Bachelor's degree in a related field and five (5) years of related experience required. Work experience may NOT substitute for education requirement. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification preferred.

Preferences

Master’s degree in social science, education, psychology, social work, or public health + 2 years of prior experience in research or program evaluation is also preferred.

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) : Hybrid Eligible