Clinical Research Coordinator - A/B (Department of Translational Medicine and Human Genetics)
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Posted Job Title
Clinical Research Coordinator - A/B (Department of Translational Medicine and Human Genetics)
Job Profile Title
Clinical Research Coordinator A
Job Description Summary
The Armellino Center of Excellence for Williams Syndrome (ACE-WS) at the University of Pennsylvania aims to provide comprehensive multidisciplinary care to individuals affected by Williams Syndrome and to facilitate research advancing the understanding and assessing potential treatments for Williams Syndrome.
Clinical Research Coordinator work includes study design, protocol development, submission to review boards, subject recruitment and enrollment, study visits and regulatory compliance in one or more studies.
Clinical Research Coordinator work includes study design, protocol development, submission to review boards, subject recruitment and enrollment, study visits and regulatory compliance in one or more studies. This position is responsible for study coordination for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects. The position involves working directly with study physicians, investigators, research nurses, and other research staff at Penn, CHOP and at other sites. Clinical Research Coordinator will recruit and perform study visits, enter data, resolve queries, facilitate specimens collection and shipment. The position will help advance the research mission of ACE-WS and show vigilance in patient safety, protocol compliance, and data quality. It requires adherence to all University of Pennsylvania, IRB, and FDA guidelines and may require working off site and flexible hours.
Clinical Research Coordinator B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting. Clinical Research Coordinator will assist with creation of master trial file and obtain the appropriate signatures for the regulatory forms. The candidate must have the ability to multi-task and be flexible. Should have excellent interpersonal skills and be able to work as part of several teams. Must be able to direct their own work and is able to work independently.
Job Description
The Armellino Center of Excellence for Williams Syndrome (ACE-WS) at the University of Pennsylvania aims to provide comprehensive multidisciplinary care to individuals affected by Williams Syndrome and to facilitate research advancing the understanding and assessing potential treatments for Williams Syndrome.
Clinical Research Coordinator work includes study design, protocol development, submission to review boards, subject recruitment and enrollment, study visits and regulatory compliance in one or more studies. This position is responsible for study coordination for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects. The position involves working directly with study physicians, investigators, research nurses, and other research staff at Penn, CHOP and at other sites. Clinical Research Coordinator will recruit and perform study visits, enter data, resolve queries, facilitate specimens collection and shipment. The position will help advance the research mission of ACE-WS and show vigilance in patient safety, protocol compliance, and data quality. It requires adherence to all University of Pennsylvania, IRB, and FDA guidelines and may require working off site and flexible hours.
In addition to the responsibilities above, the Clinical Research Coordinator B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting. Clinical Research Coordinator will assist with creation of master trial file and obtain the appropriate signatures for the regulatory forms. Must be able to direct their own work and is able to work independently.
****Position is contingent upon funding***
Qualifications
Effective problem solving abilities; effective communication and writing skills; strong organizational and time management skills; flexible and able to multi-task; demonstrated ability to work as part of a team, as well as independently; knowledge of IRB and human research protection regulations. Knowledge of RedCap preferred.
CRC-A
Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required.
CRC-B
Bachelor of Science and 2 to 4 years of experience or equivalent combination of education and experience is required.
Job Location - City, State
Philadelphia, Pennsylvania
Department / School
Perelman School of Medicine
Pay Range
$37,220.00 - $58,059.00 Annual Rate
Salary offers are made based on the candidate's qualifications, experience, skills, and education as they directly relate to the requirements of the position, as well as internal and market factors and grade profile.
Affirmative Action Statement
Penn adheres to a policy that prohibits discrimination on the basis of race, color, sex, sexual orientation, gender identity, religion, creed, national or ethnic origin, citizenship status, age, disability, veteran status, or any other legally protected class.
Special Requirements
Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.
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