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Fellows will develop an in-depth understanding of regulatory affairs and the drug development process from pre-clinical to post-marketing stages. Fellows will establish a strong foundation of expertise and knowledge to lead a successful career within the pharmaceutical industry, Food and Drug Administration (FDA), or Contract Research Organizations (CROs).
The fellowship sponsors intend for fellows to be based out of the GSK R&D Site in Upper Providence, PA or Waltham, MA throughout the 2-year duration of the fellowship program.
GSK will recruit qualified post-doctoral Regulatory Affairs fellow candidates to support either Therapeutic Groups (Regulatory Strategy), including oncology and specialty, or Chemistry Manufacturing and Controls (CMC) Biopharmaceuticals.