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Gilead Sciences
Gilead Sciences
H1B vizos rėmėjasBiotechnologijaKonsultavimasSveikatos priežiūra
„Gilead Sciences“ yra biofarmacijos įmonė, kurianti ir tiekianti vaistus gyvybei pavojingoms ligoms gydyti. Įmonė daug dėmesio skiria virusologijai, įskaitant ŽIV ir hepatitą, taip pat plečia mokslinius tyrimus onkologijos ir uždegiminių ligų srityse. Ji valdo pasaulinį daugiau nei 25 produktų ir 50 klinikinių programų portfelį, taip pat investuoja į ŽIV tyrimus ir sveikatos lygybės iniciatyvas. Darbo ieškantiems žmonėms „Gilead Sciences“ suteikia galimybių prisidėti prie mokslinių tyrimų, kūrimo ir sveikatos priežiūros programų, kuriomis siekiama gerinti pacientų gydymo rezultatus visame pasaulyje.
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Director, Ethics and Compliance Investigations

Lead Gilead’s internal investigations into ethics, compliance, fraud, and regulatory concerns. Advise leaders, strengthen hotline operations, and develop investigators.

USJungtinės ValstijosCAKalifornijaNJNaujasis Džersis
210 375 $ – 272 250 $ / metai
HibridinisVisas etatasVadovasPrivaloma Kalba: anglųAtitiktis

Aprašymas

  • Direct investigations into suspected misconduct, from fraud and conflicts of interest to healthcare professional interactions, information misuse, and other compliance or regulatory issues.
  • Interview relevant parties and examine records and data to establish the facts.
  • Prepare clear, documented conclusions and recommendations.
  • Plan and carry out investigations, identifying witnesses, records, and systems needed to gather evidence.
  • Coordinate with Legal, Employee Relations, Corporate Security, Internal Audit, and other partners.
  • Coordinate with the hotline intake team to assess, categorize, and route reported concerns.
  • Help improve hotline intake, develop metrics and dashboards, and prepare reports for the Board and business teams.
  • Keep case management records complete and up to date.
  • Ensure case closure summaries meet program requirements.
  • Spot recurring or systemic concerns and recommend changes to processes or policies.
  • Encourage ethical conduct, compliance, and speaking up.
  • Coach and support less experienced investigators.
  • Update investigation methods and tools to reflect OIG and DOJ guidance and industry practice.
  • Build an inclusive environment, grow talent, and empower teams as a people leader.

Reikalavimai

  • Bachelor’s degree with 12 years of experience, master’s degree with 10 years, or PhD with 10 years.
  • A JD or another advanced degree is preferred.
  • Experience conducting or overseeing internal investigations in a corporate, legal, or government enforcement setting.
  • Experience in healthcare, biotechnology, life sciences, or a related industry is an advantage.
  • Ability to lead sensitive investigations with discretion, independence, and professionalism.
  • Knowledge of the Foreign Corrupt Practices Act, False Claims Act, and OIG and DOJ guidance.
  • Strong interviewing, analytical, and report-writing abilities.
  • Adaptability and a commitment to continuous improvement in changing regulatory environments.
  • High ethical standards and integrity.
  • Excellent influencing, interpersonal, and communication abilities.
  • Sound judgment and the ability to put solutions into practice.
  • Strong organizational and project management abilities.
  • Ability to deliver results through others.
  • Consistent commitment to Gilead’s Core Values.

Privalumai

  • May be eligible for a discretionary annual bonus.
  • May be eligible for discretionary stock-based long-term incentives, depending on the role.
  • Paid time off.
  • Company-sponsored medical insurance.
  • Company-sponsored dental insurance.
  • Company-sponsored vision insurance.
  • Company-sponsored life insurance.
  • Reasonable accommodation support during the application process.

Susiję darbai

Erasca, Inc.

Executive Director or VP of Regulatory Affairs

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51 – 200 Darbuotojai
BiotechnologijaFarmacijos produktaiSveikatos priežiūra
USJungtinės ValstijosCAKalifornija
275 000 $ – 355 000 $ / metai
HibridinisVisas etatasVadovasPrivaloma Kalba: anglųAtitiktis

Guide global regulatory strategy for Erasca’s precision oncology medicines, from early development through approval and commercialization. Lead FDA and international health-authority engagement, submissions, and product lifecycle planning.

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Mažmeninė prekybaSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosALAlabamaAZArizonaCTKonektikutasFLFloridaKSKanzasasKYKentukisLALuizianaNJNaujasis DžersisNCŠiaurės KarolinaOHOhajasOKOklahomaPAPensilvanijaRIRod AilandasTNTenesisTXTeksasas
66 330 $ – 145 860 $ / metai
HibridinisVisas etatasVyresnysis specialistasVadovasPrivaloma Kalba: anglųAtitiktis

Oversee regulatory information requests across CVS Health operations and jurisdictions. Lead analysts and coordinate compliant responses with Legal, Compliance, and Operations.

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Executive Director, R&D Compliance, Global Medical and Scientific Affairs

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H1B vizos rėmėjasBiotechnologijaLogistikaSveikatos priežiūra
USJungtinės ValstijosNJNaujasis DžersisPAPensilvanija
231 900 $ – 365 000 $ / metai
HibridinisVisas etatasVadovasPrivaloma Kalba: anglųAtitiktis

Advise Merck’s global clinical development and medical affairs teams on pharmaceutical compliance. Oversee risk monitoring, policy implementation, senior counseling, and an international team of three.

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