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Essential Functions and Responsibilities:
- Ensure the integrity, accuracy and compliance of clinical trial data.
- Assist with the development of data edit check specifications and data listings.
- Execute data cleaning and discrepancy management to ensure compliance with the protocol.
Required Education, Skills, and Knowledge:
- At least 5 years' experience in Data Management for the pharmaceutical / biotechnology industry, or equivalent experience.
- Oncology experience is a must and RAVE database experience is preferable.
- Possesses a comprehensive understanding of regulatory guidelines and industry standards.
Work Environment:
- This job operates in a professional or remote office environment.
- Requires operating standard office equipment and keyboards.
Iovance Biotherapeutics
Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. The company is pioneering a transformational approach to treating cancer by harnessing the human immune system and is committed to continuous innovation in cell therapy.