Senior Director - Executive Director, Hematology Oncology Drug Development

Incyte Corporation; Wilmington (DE); On-site; USD 180,000 - 240,000; Full time

Job summary

Incyte Corporation in Wilmington, Delaware seeks a Senior Director - Executive Medical Director, Drug Development to drive clinical drug efforts for oncology products from Phase I to III. The role requires guiding investigator-initiated trials, upholding ethical standards, and coordinating with medical affairs for future launches.

You will liaise with regulators and external CROs to ensure successful global studies.

Qualifications

• MD/DO degree is required
• Board certification in Oncology preferred or eligible
• Ability to multi-task and work in a dynamic environment
• Excellent written and verbal communication skills

Responsibilities

• Provides guidance for investigator-initiated trials related to product development and lifecycle management.
• Maintains highest ethical and regulatory standards during investigation and development of anticancer agents.
• Collaborates with medical affairs for future anti-neoplastic agent launches.
• Detects and analyzes emergent issues in clinical drug development and develops mitigating strategies.
• Represents Incyte Corporation at national and international medical meetings and participates in advisory boards with key opinion leaders.

Education

MD/DO degree

Board certified or eligible in Oncology

Job description

Overview

A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity.

Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.

Job Summary

The Senior Director - Executive Medical Director, Drug Development is responsible for implementing clinical drug efforts for Incyte's oncology products (Phase I though Phase III).

Essential Functions of the Job

• Provides guidance for successful implementation and accomplishment of investigator-initiated trials related to product development and life cycle management of a compound.
• Implements the highest ethical and regulatory standards during the investigation and development of anticancer agents.
• Works in partnership with medical affairs for successful launch of future antineoplastic agents.
• Detects and analyzes emergent issues during clinical drug development and develops and implements mitigating strategies.
• Represents Incyte Corporation at key national and international medical and scientific meetings including participation in advisory boards with key opinion leaders.
• Liaises with discovery science to facilitate and further the development of investigational agents from a preclinical stage to clinical development.
• Serves as a source for medical and scientific expertise in oncology for outlining design strategy and execution for anti-cancer drug development.
• Collaborates with external vendors such as CROs, external imaging and laboratory resources, as well as global pharmaceutical companies for successful implementation and conduct of early phase and registration global clinical studies.
• Facilitates the development of key internal and external documents pertaining to product development including clinical study protocol, informed consents, CRFs, CSRs, meeting abstracts, scientific journal publications, strategy documents and project plans.
• Interacts with global regulatory bodies including the FDA and EMA to accomplish tasks related to oncology product development and collaborates with internal regulatory experts and oversee the clinical research plans and sections for Investigational new Drug applications (INDs) and New Drug Applications (NDAs).
• Provides medical and scientific expertise for internal cross-functional team members for development of specific anti-neoplastic agents including discovery scientists, medical scientists, biostatisticians, pharmacokineticists, pharmacovigilance and clinical operations.

Qualifications (Minimal acceptable level of education, work experience, and competency)

• M.D. or D.O. degree with a minimum of 3-5 years of experience in oncology drug development in a biotechnology or pharmaceutical company.
• Board certified or eligible in Oncology preferred.
• Ability to multi-task and work in a dynamic environment.
• Excellent written and verbal communication skills.

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Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.

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