"CLINICAL RESEARCH COORDINATOR II"

Job Description

The University of Alabama at Birmingham (UAB), Ped - Hematology/Oncology, is seeking a Clinical Research Coordinator II.

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

1. Screens and enrolls participants in clinical trials. Conducts informed consent per GCP guidelines.
2. Conducts patient visits per the protocol schedule of events. Documents adverse events, medications, and procedures conducted at each visit. Research sample collection, processing, and shipment. Administers questionnaires and other procedures as trained.
3. Documents Adverse Events (AEs) and Serious Adverse Events (SAEs) as required by protocol and regulatory guidance. Completing and submitting expedited SAE reports per protocol.
4. Conducts study initiation visits. Conducts point-of-care protocol training. Assists the PI and nursing in developing protocol orders. Attends team meetings and educational training as required.
5. Completes Case Report Forms (CRF) according to protocol. Facilitates study monitoring for data verification and query resolution. Maintains required research documentation. Conducts quality assurance activities.
6. Performs other duties as assigned.

Annual Salary Range

$50,050 - $81,330

Qualifications

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

Preferences

Experience: Knowledge of lab practices.

Knowledge, Skills, & Abilities: Knowledge of GCP and ICH Guidelines and ability to follow established regulations, procedures, and protocols. Demonstrated ability to gather data and document procedures. Ability to plan work and coordinate multiple projects.

Preferred Skills: Prefer Clinical Research experience, science and medical terminology, assisting with the coordination of research activities involved in conducting Oncology clinical trials.