The University of Alabama at Birmingham (UAB), OB/GYN - Maternal & Fetal Medicine, is seeking a Clinical Research Nurse Coordinator II (Part-Time).

General Responsibilities

• To serve as primary coordinator for clinical research studies and supporting more senior team members.
• To provide a lead role in protocol screening and participant eligibility determination working alongside other team members to ensure compliance. May provide oversight to junior clinical research coordinators (CRC) and clinical research nurse coordinators (CRNC) in review of study documents.
• To conduct all study activities in accordance with the protocol, Institutional Review Board (IRB) regulations, and Good Clinical Practice (GCP).
• To provide quality care to participants and their families within the area of clinical specialty.
• To coordinate the life cycle of the study from start-up through maintenance to closure. To manage participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
• To perform the informed consent process following GCP.
• To act as a liaison between the clinical and research staff, departments, ancillary services and the study sponsor to ensure protocol compliance throughout the study.

Key Duties & Responsibilities

1. Conducts all study activities in accordance with the protocol, IRB regulations, and GCP.
2. Coordinates the life cycle of the study from start-up through trial maintenance to closure.
3. Manages participant care including recruitment, screening, scheduling, consenting, conducting visits, and collecting various assessments such as adverse event (AE) information or questionnaires.
4. Documents and reviews medical history to determine compliance with eligibility requirements.
5. Develops/prepares study source documentation.
6. Performs the informed consent process.
7. Promotes continuity of care through consultations with participants, families, and medical and nursing staffIn collaboration with others, as needed, completes and submits Adverse Event (AE) and Serious Adverse Event (SAE) reports in a timely manner and in compliance with FDA, sponsor, and institutional policies.
8. Reports safety, clinical care and/or study conduct issues to the appropriate parties.
9. Communicates specific study requirements to internal and external parties as needed.
10. Performs clinical procedures as required by the protocol.
11. Prepares for and participates in study monitoring visits and corrects and reports findings as needed.
12. May serve as a resource person within the area of clinical expertise.
13. Administers or distributes investigational medications to study participants within the confines of the study protocol and institutional policy.
14. Uses the electronic medical record (EMR) as needed, including reporting procedure results.
15. May process and maintain lab specimens.
16. Maintains clinical records and documentation including those associated with compliant billing practices.
17. Performs other duties as assigned.

Hourly Range: $29.25 - $47.55

Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement. Currently licensed as a Registered Nurse (RN) by the Alabama Board of Nursing required.

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, religion, sexual orientation, gender identity, gender expression, 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.