CLINICAL RESEARCH COORDINATOR II
Description
The University of Alabama at Birmingham (UAB), Med - Pulmonary/Allergy/Critical Care, is seeking a Clinical Research Coordinator II.
The UAB Lung Health Center (LHC) is a nationally recognized center of excellence dedicated to improving the prevention, diagnosis, treatment, and understanding of lung diseases through groundbreaking research, innovative clinical care, and collaborative education. As part of the University of Alabama at Birmingham, one of the nation's leading academic medical centers, the Lung Health Center brings together physicians, scientists, clinical research professionals, and healthcare experts committed to transforming lung health outcomes locally and globally. Our multidisciplinary teams work across pulmonary medicine, critical care, translational science, population health, and clinical research to address some of the most pressing challenges in respiratory health, including chronic obstructive pulmonary disease (COPD), asthma, interstitial lung disease, pulmonary fibrosis, lung cancer, pulmonary vascular disease, and emerging respiratory conditions. Our mission is to advance lung health through discovery, innovation, education, and compassionate care while developing the next generation of healthcare and research professionals.
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
Collects and records preliminary data for clinical research programs.
Recruits and performs follow-up visits and phone calls with research participants as protocols outline.
Schedules visits according to research protocols.
Coordinates protocol, lab, and fieldwork.
Prepares for and participates in study monitoring visits.
Corrects findings, and completion of reports, and corresponds with sponsors.
Completes Case Report Forms (CRF) according to protocol.
Assists with development of protocols and standard operating procedures (SOPs) for data quality assurance.
Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of supplies/materials).
Performs a variety of medical procedures under supervision.
Assists in compiling, editing, and proofreading written reports for both internal and external stakeholders.
Uses Electronic Data Capture (EDC) systems necessary for operations.
Performs other duties as assigned.
Annual Salary Range\: $50,050 - $81,330