Vice President, Product Development - Hematology

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POST DATE 8/18/2016
END DATE 12/19/2016

United Therapeutics Durham, NC

Durham, NC
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Full Time
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The VP, Product Development is responsible for conceptualizing, designing, developing and executing all aspects (CMC, preclinical, clinical, manufacturing, QA, post-marketing) of the development of a product or products to ensure the successful submission and approval by the FDA and other regulatory agencies. This is a hands on position, requiring dynamic leadership and the knowledge required to implement and oversee advanced clinical trials, and set the strategy for regulatory submission. This person will have full responsibility for the content of all regulatory submissions for the given product.


* Provide cross-functional and matrix leadership to project team, ensuring strategic planning, design, conduct, analysis and reporting of clinical trials and maintains scientific merit and regulatory compliance, leading up to product approval
* Manage all project planning, including timelines, budgets, and resourcing
* Act as the key point of contact with Steering Committees, Advisory Committees, Data Monitoring Committees, and Publication Committees
* Organize and manage all aspects of preclinical or clinical studies alone or in conjunction with a preclinical scientist, clinical or senior clinical research scientist, study manager, and/or clinical research associates
* Provide scientific insight into study design, serving as the subject matter expert in Hematology
* Develop and write clinical protocols and Investigator's Brochures
* Participate with clinical team in planning & conduct of investigator meetings, advisory boards, and other clinical/scientific interactions
* Responsible for selection of clinical sites/CRO, development valid medical license strongly preferred
* Demonstrated understanding of the overall drug development process with clinical trial design, study implementation, sponsor/site interactions, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies to be reviewed by Health Authorities
* 12+ years of full life cycle product development experience - 8 + years hands on experience managing across phase 1-4 clinical trials as well as registration trials
* Thorough knowledge of GCP, ICH and PhRMA Guidelines
* Thorough knowledge of relevant FDA regulations and guidelines; demonstrated experience interacting with FDA personnel; knowledge of EU regulations and guidelines a plus
* Ability to travel as required, typically around 25%


* Medical specialty training preferred in Hematology
* A proven track record of driving a Hematology product from proof of concept to regulatory approval and commercialization
* Strong communication (oral and written), presentation, and analytical skills
* Ability to work independently, prioritize tasks efficiently and meet expected time frames
* Ability to interact collaboratively with various departments, regulatory agencies and investigators
* Previous experience successfully progressing a product from clinical trial through the regulatory approval process strongly preferred
* Proficiency with Microsoft Office products

United Therapeutics Corporation is an Equal Opportunity/Affirmative Action Employer - EOE Minorities / Females / Protected Veterans / Individuals with Disabilities