What are the responsibilities and job description for the Clinical Research Coordinator I (Temp) position at University of Alabama at Birmingham?
The Nutrition for Precision Health Study, conducted by the University of Alabama at Birmingham (UAB), is currently in need of a Clinical Research Coordinator I. The goal of the study is to gain insight into how individuals respond to food, in order to prevent and combat health conditions that are impacted by nutrition. This position will assist with coordinating study visits, data collection and data entry. This position will be full-time on UAB's campus with split work at the Webb building and the Clinical Research Unit in Jefferson Tower. Primary Responsibilities Coordinate in-person study visits with research participants and set up necessary supplies. Collect physical measures (height, weight, etc.) and vital signs (blood pressure, oral temperature, etc) during participant clinic visits. Input data into electronic data capture systems. Perform other duties as assigned.
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
Primary Location
Temporary Services
Job Category
UAB Temporary Services
Organization
114402000 Temporary Services
Employee Status
Temporary
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.
Key Duties & Responsibilities
- Collects and documents data for clinical research programs. Recruits and performs follow-up with research participants as protocols outline. Schedules visits according to research protocols.
- Assists in coordination of lab and fieldwork. Coordinates appointments for additional procedures as necessary. Prepares for and participates in study monitoring visits. Assists with correcting findings. Participates in study meetings and conference calls.
- Assists with the completion of Case Report Forms (CRF) according to protocol.
- May assist with development of protocols and standard operating procedures (SOPs) for data quality assurance.
- Performs administrative duties in support of research conduction as needed.
- Prepares source documentation for review with investigators. May perform a variety of medical procedures under supervision.
- May assist in compiling, editing, and proofing written reports for both internal and external administrative offices. May perform data analysis using a variety of software packages.
- May use Electronic Data Capture (EDC) systems necessary for operations under supervision.
- Performs other duties as assigned. Minimum Requirements High School diploma or GED required.
Primary Location
Temporary Services
Job Category
UAB Temporary Services
Organization
114402000 Temporary Services
Employee Status
Temporary
Shift
Day/1st Shift
Work Arrangement (final schedule to be determined by the department/hiring manager)
Onsite