Uofmhealth
Clinical Research Coord Assoc/Technician
The division of Pediatric Pulmonology is seeking a skilled clinical research coordinator to support studies for multiple faculty across the division.
Mission Statement The mission of the University of Michigan is to serve the people of Michigan and the world through preeminence in creating, communicating, preserving and applying knowledge, art, and academic values, and in developing leaders and citizens who will challenge the present and enrich the future.
What Benefits can you Look Forward to?
Excellent medical, dental and vision coverage effective on your very first day
2:1 Match on retirement savings
Responsibilities This position may provide study coordination for multiple clinical research studies, depending on the complexity that range from moderate to complex. Coordinator experience and mastery of all job duties from previous job description is required. This position should be able to perform tasks and make decisions independently, consistently, and accurately, and demonstrate that they have achieved a moderate level of expertise in all of their skills and abilities, resulting in high-quality work. It is presumed that this position is able to apply their skills to a broad range of different types of clinical studies, navigate available resources appropriately, effectively use all tools and job aids at their disposal and operate clinical technologies with a reasonable degree of proficiency. This position can perform the majority of tasks independently and perform quality checks of their work. They also know where and how to identify appropriate resources and support and are able to discern when to elevate issues needing additional intervention. Key behavioral competency descriptors include: demonstrate, implement, execute, and use.
Key Duties Include
Working as part of a team to develop and implement clinical research protocols, preparing proposals for IRB approval and communication with the IRB on amendments and compliance reporting
Screening patients for enrollment in studies
Obtaining consent for inclusion in research studies
Communicating with families enrolled in studies to maintain engagement
Conducting study activities, which may include conducting surveys/interviews, and facilitating biologic sample collection
Ensuring integrity of data and biological specimen collection, preliminary processing, and documentation
Gathering and input of information from the electronic medical record (EPIC/MiChart) and research databases (e.g. RedCAP)
Managing database queries and resolving gaps in data collection
Resolving simple questions that come up during research protocols
Required Qualifications
Bachelor's degree in Health Science or equivalent in combined education and clinical research experience
Certification is required through Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Association (SOCRA) as a Certified Clinical Research Professionals (CCRP) or equivalent. Candidates must be eligible to register or take the exam at date of hire and the certification must be completed or passed within six months of date of hire.
Minimum 2 years of directly related experience in clinical research and clinical trials is necessary.
Clinical Research Technician Qualifications
Associate degree in Health Science or an equivalent combination of related education and experience is necessary
Minimum 1 year of directly related experience in clinical research and clinical trials is necessary.
Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.
Desired Qualifications
Experience with IRB and RedCap preferred
Understanding of medical terminology preferred
Modes of Work Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment.
Underfill Statement This position may be underfilled at a lower classification depending on the qualifications of the selected candidate.
Additional Information This description is intended to indicate the kinds of tasks and levels of work difficulty that will be required of positions that will be given this title and shall not be construed as declaring what the specific duties and responsibilities of any particular position shall be. It is not intended to limit or in any way modify the right of any supervisor to assign, direct, and control the work of employees under his supervision. The use of a particular expression or illustration describing duties shall not be held to exclude other duties not mentioned that are of a similar kind or level of difficulty.
SUPERVISION RECEIVED This position should report directly to a Clinical Research Coordinator Lead, Clinical Research Project Manager, Administrator, or Faculty Principal Investigator.
SUPERVISION EXERCISED None
Background Screening Michigan Medicine conducts background screening and pre‑employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre‑employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U‑M campuses.
Application Deadline Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled anytime after the minimum posting period has ended.
U‑M EEO Statement The University of Michigan is an equal employment opportunity employer.
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Mission Statement The mission of the University of Michigan is to serve the people of Michigan and the world through preeminence in creating, communicating, preserving and applying knowledge, art, and academic values, and in developing leaders and citizens who will challenge the present and enrich the future.
What Benefits can you Look Forward to?
Excellent medical, dental and vision coverage effective on your very first day
2:1 Match on retirement savings
Responsibilities This position may provide study coordination for multiple clinical research studies, depending on the complexity that range from moderate to complex. Coordinator experience and mastery of all job duties from previous job description is required. This position should be able to perform tasks and make decisions independently, consistently, and accurately, and demonstrate that they have achieved a moderate level of expertise in all of their skills and abilities, resulting in high-quality work. It is presumed that this position is able to apply their skills to a broad range of different types of clinical studies, navigate available resources appropriately, effectively use all tools and job aids at their disposal and operate clinical technologies with a reasonable degree of proficiency. This position can perform the majority of tasks independently and perform quality checks of their work. They also know where and how to identify appropriate resources and support and are able to discern when to elevate issues needing additional intervention. Key behavioral competency descriptors include: demonstrate, implement, execute, and use.
Key Duties Include
Working as part of a team to develop and implement clinical research protocols, preparing proposals for IRB approval and communication with the IRB on amendments and compliance reporting
Screening patients for enrollment in studies
Obtaining consent for inclusion in research studies
Communicating with families enrolled in studies to maintain engagement
Conducting study activities, which may include conducting surveys/interviews, and facilitating biologic sample collection
Ensuring integrity of data and biological specimen collection, preliminary processing, and documentation
Gathering and input of information from the electronic medical record (EPIC/MiChart) and research databases (e.g. RedCAP)
Managing database queries and resolving gaps in data collection
Resolving simple questions that come up during research protocols
Required Qualifications
Bachelor's degree in Health Science or equivalent in combined education and clinical research experience
Certification is required through Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Association (SOCRA) as a Certified Clinical Research Professionals (CCRP) or equivalent. Candidates must be eligible to register or take the exam at date of hire and the certification must be completed or passed within six months of date of hire.
Minimum 2 years of directly related experience in clinical research and clinical trials is necessary.
Clinical Research Technician Qualifications
Associate degree in Health Science or an equivalent combination of related education and experience is necessary
Minimum 1 year of directly related experience in clinical research and clinical trials is necessary.
Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.
Desired Qualifications
Experience with IRB and RedCap preferred
Understanding of medical terminology preferred
Modes of Work Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment.
Underfill Statement This position may be underfilled at a lower classification depending on the qualifications of the selected candidate.
Additional Information This description is intended to indicate the kinds of tasks and levels of work difficulty that will be required of positions that will be given this title and shall not be construed as declaring what the specific duties and responsibilities of any particular position shall be. It is not intended to limit or in any way modify the right of any supervisor to assign, direct, and control the work of employees under his supervision. The use of a particular expression or illustration describing duties shall not be held to exclude other duties not mentioned that are of a similar kind or level of difficulty.
SUPERVISION RECEIVED This position should report directly to a Clinical Research Coordinator Lead, Clinical Research Project Manager, Administrator, or Faculty Principal Investigator.
SUPERVISION EXERCISED None
Background Screening Michigan Medicine conducts background screening and pre‑employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre‑employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U‑M campuses.
Application Deadline Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled anytime after the minimum posting period has ended.
U‑M EEO Statement The University of Michigan is an equal employment opportunity employer.
#J-18808-Ljbffr