Senior Director, Clinical Science

April 6

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Iovance Biotherapeutics, Inc.

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Iovance Biotherapeutics, Inc. is pioneering a transformational approach to treating cancer by harnessing the human immune system's ability to recognize and attack diverse cancer cells in each patient. The company focuses on T-cell-based immunotherapy, specifically Tumor Infiltrating Lymphocyte (TIL) therapy, which involves reinvigorating a patient’s TILs to fight cancer. Iovance's TIL therapy is being investigated in clinical trials across multiple advanced solid tumor cancers. Additionally, the company is advancing genetically modified TIL therapies and exploring potential applications of PBL (peripheral blood lymphocyte) therapy for blood cancers. As a leader in cell therapy, Iovance owns a state-of-the-art Cell Therapy Center in Philadelphia for manufacturing their therapies using proprietary GMP. The company is at the forefront of developing personalized and patient-specific cancer treatments.

Immuno Oncology • Autologous Cell Therapy • Tumor Infiltrating Lymphocytes (TIL) • Novel Cancer Immunotherapies • cell therapy

501 - 1000 employees

Founded 2014

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

📋 Description

• Participates in development of Clinical Development plans (CDPs) • Supports Medical Directors/Clinical Science Physicians with clinical documentation • Represents Clinical Science on various teams/sub-teams • Supports training and interactions with study site personnel • Maintains scientific and clinical knowledge in relevant therapeutic and disease area(s) • Collaborates with internal and external partners • Provides clinical science support for assigned studies and programs • Participates in ongoing cross functional meetings

🎯 Requirements

• 12+ years’ clinical trial experience with relevant therapeutic area experience • Data table figure listing review experience is mandatory • Experience with authoring clinical study protocols and summarizing study results and conclusions • In-depth understanding of Phase 1 through 4 drug development • Strong analytical skills, especially with regard to understanding and interpreting scientific research, literature and clinical trial data • Comprehensive understanding of product and safety profiles • Sound knowledge of medical aspects of GCP (Good Clinical Practice), ICH (International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use), FDA, EMEA, NICE and other relevant guidelines and regulations • Strong computer skills, including Microsoft Office Suite (Word, PowerPoint and Excel) • Good business acumen; has working knowledge of the multidisciplinary functions involved in a company’s drug development process, e.g. clinical operations, biostatistics, regulatory, commercial operations, etc. • Excellent project management skills: can prioritize multiple tasks and goals and ensure the timely, on-target and within-budget accomplishment • Good interpersonal, verbal communication and influencing skills; can influence without authority • Strong written communication skills • Good business presentation skills; is comfortable and effective when presenting to others, internally or externally • Good judgment and decision-making skills; Team player