Senior /Vice President, Clinical Research, CD4+CD8; Oncology

NY Biotech

Responsibilities/Requirements

• Provide therapy area medical and scientific expertise, translating complex scientific concepts and data while providing a strategic point of view. 
• Execute the planning and management of innovative clinical trials, study design, trial management, and interpretation of trial results. 
• Engage and inspire the cross-functional program teams through communication of strategic plans and vision. 
• Cultivate and nurture strong collaborations, relationships, and support with Investigators, Academic partners and KOLs. 
• Partner with Business Development to evaluate the scientific and strategic value of the external collaboration opportunities. 
• Prepare, estimate, and manage the section budget, proposing priorities to management and ensures the allocation of resources. 
• Lead, supervise, and facilitate the professional training and development of the physician team; conduct reviews and evaluate the performance and compensation of direct reports. 


Basic Qualifications:

Qualification and Education Requirements 
• MD with 6+ years of pharmaceutical or biotechnology industry experience in oncology clinical development; experience in early phase development. 
• Expertise in clinical hematological malignancies; fellowship trained Hematologist or Hematologist/Oncologist. 
• Experience designing, conducting Phase 1-2 clinical trials in oncology. 
• Proven experience in leading project and clinical study teams in industry setting. 
• Understanding of cellular immunology and typical assay systems for same 


Qualified candidates should email CV/Resume to jobs@tseworldwide.com