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Responsibilities:

  • Works closely with functional leaders to create optimal development paths for product candidates.
  • Plans, manages, and creates Clinical Trial Applications, Market Applications, and amendments.
  • Leads cross-functional teams in preparing for health authority meetings.

Requirements:

  • BS degree in life sciences with minimum 10 years’ experience in regulatory affairs.
  • Late-stage experience in oncology drug development.
  • Able to write and edit high-quality clinical-regulatory documents.

Work Environment:

  • This job operates in a professional or remote office environment.
  • Must be able to remain in a stationary position for prolonged periods and operate standard office equipment.

Iovance Biotherapeutics

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. They are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer.

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