University of Alabama at Birmingham
CLINICAL RESEARCH COORDINATOR I
University of Alabama at Birmingham, Birmingham, Alabama, United States, 35275
Job Description - CLINICAL RESEARCH COORDINATOR I (T231975)
CLINICAL RESEARCH COORDINATOR I - ( T231975 )
Description The University of Alabama at Birmingham (UAB), Med - Cardiovascular Disease, is seeking a Clinical Research Coordinator I.
General Responsibilities To serve as coordinator for studies and provide support to other team members within the даара 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-Za recording data, recruiting and performing follow-up with participants, scheduling visits and assisting in coordination of lab and fieldwork.
Key Duties & Responsibilities
Recruit, screen, consent, and enroll participants.
Implements study participant recruiting and screening protocols.
Meets recruitment and enrollment goals.
Collects, analyzes, and enters data for clinical trials.
Completes enrollment logs, informed consent logs, and all other data forms with high accuracy and attention to detail.
Uses REDCap and SPSS databases to enter and summarize study data.
Manages all aspects of assigned clinical studies, including education.
Schedules visits according(prop) to research protocols.
Performs follow-up with research participantsución.
Ensures that documents such as eligibility forms and informed consent are appropriately gathered and maintained.
Monitors compliance of study procedures with federal, state, and university regulations.
Ensures IRB, Good Clinical Practice, and HIPAA regulations are followed.
Assists with regulatory submissions and duties.
Assists in the coordination of lab work.
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.
Effectively and professionally communicates sensitive information and maintains confidentiality.
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 HIP significativa regulations.
Strong attention to detail for accurate data collection and documentation.
Excellent interpersonal and communication skills forassemblage patient interaction.
Ability to work independently with minimal supervision while managing multiple studies
At least 1 year of clinical research experience preferred.
UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.
Primary Location University
Job Category Clinical Research
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
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Description The University of Alabama at Birmingham (UAB), Med - Cardiovascular Disease, is seeking a Clinical Research Coordinator I.
General Responsibilities To serve as coordinator for studies and provide support to other team members within the даара 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-Za recording data, recruiting and performing follow-up with participants, scheduling visits and assisting in coordination of lab and fieldwork.
Key Duties & Responsibilities
Recruit, screen, consent, and enroll participants.
Implements study participant recruiting and screening protocols.
Meets recruitment and enrollment goals.
Collects, analyzes, and enters data for clinical trials.
Completes enrollment logs, informed consent logs, and all other data forms with high accuracy and attention to detail.
Uses REDCap and SPSS databases to enter and summarize study data.
Manages all aspects of assigned clinical studies, including education.
Schedules visits according(prop) to research protocols.
Performs follow-up with research participantsución.
Ensures that documents such as eligibility forms and informed consent are appropriately gathered and maintained.
Monitors compliance of study procedures with federal, state, and university regulations.
Ensures IRB, Good Clinical Practice, and HIPAA regulations are followed.
Assists with regulatory submissions and duties.
Assists in the coordination of lab work.
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.
Effectively and professionally communicates sensitive information and maintains confidentiality.
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 HIP significativa regulations.
Strong attention to detail for accurate data collection and documentation.
Excellent interpersonal and communication skills forassemblage patient interaction.
Ability to work independently with minimal supervision while managing multiple studies
At least 1 year of clinical research experience preferred.
UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.
Primary Location University
Job Category Clinical Research
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
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