Clinical Research Coordinator B (Cardiovascular Institute)
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Posted Job Title
Clinical Research Coordinator B (Cardiovascular Institute)
Job Profile Title
Clinical Research Coordinator B
Job Description Summary
This position is in the Cardiac Electrophysiology Department which treats and studies the electrical component of the heart by way of ablation procedures and/or cardiac device implants (internal cardioverter defibrillator, pacemaker). The research coordinator will assist in the management of multiple clinical trials and will be responsible for study coordination for industry studies, investigator-initiated studies, and multi-center research studies. They will facilitate, promote and ensure good clinical practice in the conduct of all research protocols in the Department. They will coordinate the screening of subjects, subject enrollment, collection and storage of biological samples with related study documents, the collection of clinical data and data entry. Independently manage different phases of clinical trials. They may assist with Institutional Review Board (IRB) filings, sponsor and investigator filings and research related presentations. Participate in study team meetings, site group meetings and ongoing protocol training/compliance meetings. They will work closely with the Principal Investigator, research manager, and study team to identify problems and develop solutions. They will adhere to all University and other regulatory guidelines.
Job Description
This position is contingent upon favorable funding.
This position is in the Cardiac Electrophysiology Department which treats and studies the electrical component of the heart by way of ablation procedures and/or cardiac device implants (internal cardioverter defibrillator, pacemaker). The research coordinator will assist in the management of multiple clinical trials and will be responsible for study coordination for industry studies, investigator-initiated studies, and multi-center research studies. They will facilitate, promote and ensure good clinical practice in the conduct of all research protocols in the Department. They will coordinate the screening of subjects, subject enrollment, collection and storage of biological samples with related study documents, the collection of clinical data and data entry. Independently manage different phases of clinical trials. They may assist with Institutional Review Board (IRB) filings, sponsor and investigator filings and research related presentations. Participate in study team meetings, site group meetings and ongoing protocol training/compliance meetings. They will work closely with the Principal Investigator, research manager, and study team to identify problems and develop solutions. They will adhere to all University and other regulatory guidelines.
Qualifications
Bachelor's Degree with 2-3 years of related experience in research and clinical study methodologies or equivalent combination of education and experience is required
Working Conditions
Office, Library, Computer Room; Requires extensive safety
Physical Effort
Typically sitting at a desk or table; Occasional lifting 25 lb. or less
Job Location - City, State
Philadelphia, Pennsylvania
Department / School
Perelman School of Medicine
Pay Range
$43,919.00 - $52,661.00 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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