Senior Regulatory Affairs Specialist (Office of Clinical Research)
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Posted Job Title
Senior Regulatory Affairs Specialist (Office of Clinical Research)
Job Profile Title
Regulatory Affairs Specialist Senior
Job Description Summary
Regulatory Affairs Specialist Senior
The primary responsibility of the Regulatory Affairs Senior Specialist is to support faculty Sponsors and serve as the project and regulatory lead for university held INDs, IDEs, and foreign CTAs. In this role, he/she will provide Sponsor clinical operations leadership, contribute to and review core documents, provide project management to Sponsor teams including management of the Sponsor trial master file, and prepare Health Authorities submissions. In addition, he/she will provide day-to-day project support and contribute to the development of operational processes, that will ensure adherence to government and institutional policies and provide guidance to current and potential Sponsors in Perelman School of Medicine (PSOM).
This position will support, train and qualify potential IND/IDE/CTA Sponsors of Investigator Initiated Trials throughout the clinical trial life cycle. He/she will aid with the development of Sponsor documents (consent forms, safety monitoring plans, investigator brochures, safety reporting etc.) and Sponsor responsibilities.
Prior experience in drug or device clinical trials and experience implementing ICH regulations is required. Project management experience is essential.
Job Description
Regulatory Affairs Specialist Senior
The primary responsibility of the Regulatory Affairs Senior Specialist is to support faculty Sponsors and serve as the project and regulatory lead for university held INDs, IDEs, and foreign CTAs. In this role, he/she will provide Sponsor clinical operations leadership, contribute to and review core documents, provide project management to Sponsor teams including management of the Sponsor trial master file, and prepare Health Authorities submissions. In addition, he/she will provide day-to-day project support and contribute to the development of operational processes, that will ensure adherence to government and institutional policies and provide guidance to current and potential Sponsors in Perelman School of Medicine (PSOM).
This position will support, train and qualify potential IND/IDE/CTA Sponsors of Investigator Initiated Trials throughout the clinical trial life cycle. He/she will aid with the development of Sponsor documents (consent forms, safety monitoring plans, investigator brochures, safety reporting etc.) and Sponsor responsibilities.
Prior experience in drug or device clinical trials and experience implementing ICH regulations is required. Project management experience is essential.
Required: Resume and cover letter required with application.
COVID-19 vaccination is a requirement for all employees at the University of Pennsylvania. New hires are expected to be fully vaccinated before beginning work at the University.
Salary: The job pay range encompasses the full range of employees from new hires to the salaries of Penn employees with many years of experience and seniority and is not a precise indicator of salaries of new hires when looking at the top end. Based on what we pay employees coming into this position our pay range is $70,000-$85,000 based on education and experience above the minimum qualifications.
Job Location - City, State
Philadelphia, Pennsylvania
Department / School
Perelman School of Medicine
Pay Range
$59,703.00 - $95,524.33
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.
University Benefits
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