306886true306886falseSubmission for the position CLINICAL RESEARCH COORDINATOR II - Job Number T231968false306886falsetrueCLINICAL RESEARCH COORDINATOR IIT231968 The University of Alabama at Birmingham UAB Med - Cardiovascular Disease 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 We are seeking a Clinical Research Coordinator II to perform some of or all of the following duties and responsibilities depending on the candidates 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 suppliesmaterials. 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. Annual Salary Range 50050 - 81330 The University of Alabama at Birmingham UAB Med - Cardiovascular Disease 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 We are seeking a Clinical Research Coordinator II to perform some of or all of the following duties and responsibilities depending on the candidates 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 suppliesmaterials. 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. Annual Salary Range 50050 - 81330 Bachelors 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. UAB is an Equal EmploymentEqual 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 veterans 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 UABs Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edutitleix. Bachelors 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. UAB is an Equal EmploymentEqual 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 veterans 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 UABs Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edutitleix.