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Associate Director, Global Compliance

at Incyte Corporation in Wilmington, Delaware, United States

Job Description

Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value.
The Company strives to discover and develop first-in-class and best-in-class medicines-advancing a diverse portfolio of large and small molecules.
Job Summary (Primary function)
The Associate Director, Global Compliance supports the management of Incyte's Global Corporate Compliance Program, with significant interaction with Incyte's Global and Regional functions, Country Management, and other functions, such as Global Scientific, Medical Affairs, Clinical Development, Strategy and Corporate Development, and Technical Operations. The Associate Director works to continuously enhance Incyte's Compliance Program through application of best practices in the life sciences Compliance space.
Essential Functions of the Job (Key responsibilities)
Support the development, enhancement, and implementation of Incyte's Compliance Program elements across regions, markets, and corporate functions with a view toward global harmonization.
Promote and implement enhanced Compliance Program elements within relevant regions, markets, and corporate functions, including determining effective controls at the global and functional level.
Establish collaborative relationships with leaders of relevant regions, markets, and corporate functions and contribute to the development of Compliance annual plans and priorities based on risk assessments, leadership feedback, and other relevant inputs.
Draft, coordinate, and implement global, regional, and/or local Compliance policies, SOPs, and other Compliance tools and templates.
Support development and delivery of live and/or recorded Compliance training.
Support Global Compliance efforts by participating in the design and development of Compliance monitoring activities.
Conduct Compliance reviews of certain business activities, e.g. external funding requests.
Represent Compliance at key business meetings and industry events.
Provide ongoing support to general Compliance projects and processes as necessary.
Support Incyte's global anti-bribery anti-corruption (ABAC) program, including policy, training and process needs.
Manage and implement enhancements to Incyte's third party due diligence processes, including management of systems, third party risk criteria, ordering and review of diligence, developing mitigation actions in collaboration with the business, and ongoing monitoring of higher risk third parties.
Work cross-functionally to support Incyte's efforts to continuously enhance third party management.
Support development and implementation of new Compliance programs in new markets.
Assist in development and implementation of Compliance plans for new affiliates and/or partners in new, global markets.
Provide guidance to new affiliates and/or partners, and integrate compliance controls into the scope of these businesses as applicable with a focus on global harmonization and "right sizing" the program.
Maintain a current working knowledge of various laws, regulations, and industry guidance that affect the Global Compliance Program, including federal and state government price reporting laws, state and federal privacy laws including GDPR, fraud and abuse and anti-kickback statutes, OIG guidelines, industry codes in relevant markets including PhRMA, EFPIA and JPMA, US state marketing compliance laws, FCPA, UK Bribery Act and other anti-bribery laws.
Contribute positively to a strong culture of compliance and ethics.
Qualifications (Minimal acceptable level of education, work experience, and competency)
Bachelor's degree required.
Minimum of 10 years of compliance experience in the pharmaceutical and life sciences industry preferred.
Experience in the areas of global compliance best practices, including working in markets outside the United States or with R&D/Medical functions within the pharmaceutical industry.
Knowledge of and experience with laws, regulations, and industry guidance that affect the pharmaceutical industry.
Effective public speaking skills and an ability to communicate in both verbal and written form with multiple stakeholders within and outside the company.
Collaborative team player with ability to work effectively with cross functional teams and projects both within... For full info follow application link.

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Job Posting: 1084031

Posted On: Dec 08, 2022

Updated On: Jan 07, 2023

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