Associate Medical Director

Responsibilities

• Serve as the primary clinical contact for IOVANCE clinical trials
• Direct protocol implementation including site identification and investigator communication
• Co-manage program development and collaborate cross-functionally with clinical, manufacturing, regulatory, and medical affairs teams
• Monitor clinical trials, overseeing trial conduct, safety, and CRO medical monitors
• Support data analysis, IDMC meetings, interim analyses, and clinical study report writing
• Contribute to the preparation of abstracts, presentations, and manuscripts

Requirements

• Board Certified MD
• Minimum of 1-2 years of oncology clinical trials experience
• Effective oral and written communication skills
• Ability to work independently in a fast-paced environment

Preferred Qualifications

• Hematology/Oncology subspecialty
• Subspecialty training in oncology and/or hematopoietic transplantation
• Significant clinical trial experience and outstanding academic achievement

About the Company

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells.