What are the responsibilities and job description for the CLINICAL RESEARCH COORDINATOR II (2) position at University of Alabama at Birmingham?
The University of Alabama at Birmingham (UAB), OB/GYN - Maternal & Fetal Medicine, is seeking a Clinical Research Coordinator II.
General Responsibilities
Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement.
Preferences
Primary Location
University
Job Category
Clinical Research
Organization
311551600 OB/GYN - Maternal & Fetal Medicine
Employee Status
Regular
Shift
Day/1st Shift
Work Arrangement (final schedule to be determined by the department/hiring manager)
Onsite
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.
- Serves as a liaison with medical staff, University Departments, ancillary departments, and/or satellite facilities.
- Organizes patient enrollment planning.
- Conducts quality assurance activities.
- Compiles and analyzes data.
- Develops and implements procedures, maintains records, tracks progress, and conducts quality assurance on data collected.
- Maintains compliance with federal, state, and accrediting agencies (sponsors).
- Maintains any required documentation.
- Coordinates patient care and/or patient follow-up functions of the clinical study including planning and developing related activities.
- Arranges access to study medications, including authorization for prescriptions.
- Employs strategies to maintain recruitment and retention rates.
- Prepares and submits multiple levels of research documentation (i.e. IRB, IND, or FDA submissions, educational materials, reports, grant renewal reports, and study forms).
- Manages investigational products (IP).
- Employs the required system (including personnel) for handling, dispensing, and documenting IP for sponsored protocols.
- In conjunction with Investigators, plans and implements the clinical protocol's goals and objectives.
- Compiles, edits, and proofs written reports for both internal and external administrative offices.
- Provides data for the creation of study budgets as needed.
- Completes Case Report Forms (CRF) according to protocol.
- Assists with the development of standard operating procedures (SOPs) for data quality assurance.
- Performs vendor analysis and equipment configuration as needed.
- May perform a variety of medical procedures.
- Under the oversight of the Investigator, develops protocols, identifies efficiencies, and improves processes.
- Arranges multidisciplinary evaluations.
- Processes and maintains lab specimens and manages site supplies as needed.
- Serves as a mentor to junior staff, including student assistants.
- Performs other duties as assigned.
Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement.
Preferences
- Effective verbal and written communication skills, as well as a willingness to work within a group setting.
Primary Location
University
Job Category
Clinical Research
Organization
311551600 OB/GYN - Maternal & Fetal Medicine
Employee Status
Regular
Shift
Day/1st Shift
Work Arrangement (final schedule to be determined by the department/hiring manager)
Onsite
Salary : $50,050 - $81,330
CLINICAL RESEARCH REGULATORY COORDINATOR II
UAB Health System -
Birmingham, AL
CLINICAL RESEARCH NURSE COORDINATOR II
UAB Health System -
Birmingham, AL