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Regulatory Specialist

Company: Aerotek
Location: Newark
Posted on: January 15, 2022

Job Description:

Remote Regulatory Position - Must be a resident of PA, NJ, or DEDescription:Process all initial regulatory documents for submission to the Pharmaceutical Sponsors and Institutional Review Board (IRB)Prepare and process all regulatory documentation through the IRB, CTSRMC, FDA and all applicable regulatory review committeesPrepare and process all required regulatory documentation for pharmaceutical companies, contract research organizations (CROs), the NCI and the FDA.Additional Skills & Qualifications:MUST HAVE Experience submitting to the IRB a minimum of 10 timesA Bachelors Degree and 2 years to 5 years of experience or equivalent combination of education and experience is required.1-3 years relevant experience in an academic regulatory environment Remote Regulatory Position - Must be a resident of PA, NJ, or DE#LI-AM1 About Actalent:Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. Were supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Keywords: Aerotek, Newark , Regulatory Specialist, Other , Newark, New Jersey

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