What are the responsibilities and job description for the CLINICAL RESEARCH COORDINATOR II position at University of Alabama at Birmingham?
The University of Alabama at Birmingham (UAB), Med - Cardiovascular Disease, is seeking a Clinical Research Coordinator II.
General Responsibilities
We are seeking a Clinical Research Coordinator II to perform some of or all of the following duties and responsibilities, depending on the candidate's experience level:
Bachelor's degree in a related field and three (3) years of related experience required. Work experience may substitute for education requirement.
Preferences
Organization
311401000 Med - Cardiovascular Disease
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.
We are seeking a Clinical Research Coordinator II to perform some of or all of the following duties and responsibilities, depending on the candidate's experience level:
- Recruits, screens, consents, and enrolls participants.
- Implements study participant recruiting and screening protocols.
- Meets recruitment and enrollment goals.
- Manages all aspects of assigned clinical studies, including education.
- Collects, analyzes, and enters data for clinical trials and ensures quality control.
- Completes enrollment logs, informed consent logs, and all other data forms with high accuracy and attention to detail.
- Assists in the coordination of lab work.
- Prepares for study monitoring visits.
- Ensures that documents such as eligibility forms and informed consent are appropriately gathered and maintained, and IRB-, Good Clinical Practice-, and HIPAA regulations are followed.
- Uses REDCap and SPSS databases to enter and summarize study data.
- Monitors compliance of study procedures with federal, state, and university regulations.
- Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials).
- Works with minimal supervision, plans, organizes, and coordinates multiple work assignments, and establishes and maintains effective working relationships with others.
- Effectively and professionally communicates sensitive information and maintains confidentiality.
- Assist with regulatory submissions and duties.
- 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
- Previous clinical research experience, particularly in cardiovascular studies.
- Familiarity with REDCap and SPSS databases for data entry and analysis.
- Experience with Good Clinical Practice (GCP) guidelines and regulatory compliance.
- Knowledge of IRB processes and HIPAA regulations.
- Strong attention to detail for accurate data collection and documentation.
- Excellent interpersonal and communication skills for patient interaction.
- Ability to work independently with minimal supervision while managing multiple studies.
Organization
311401000 Med - Cardiovascular Disease
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