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MSD
MSD
Sponzor vizuma H1BBiotehnologijaLogistikaZdravstveno varstvo

MSD je globalno biofarmacevtsko podjetje, ki razvija zdravila in cepiva za reševanje ključnih zdravstvenih izzivov, vključno z rakom, nalezljivimi boleznimi, srčno-žilnimi in presnovnimi stanji ter preventivno zdravstveno oskrbo. V Združenih državah Amerike, Kanadi in Portoriku je znano kot Merck & Co., Inc. MSD združuje znanstvene raziskave s strokovnim znanjem na področju razvoja in trženja, da bi zdravstvene rešitve približalo ljudem in živalim.

Njegovo delo zajema zdravje ljudi, zdravje živali ter raziskave in razvoj, kar ustvarja priložnosti za strokovnjake v znanstvenih, kliničnih, komercialnih, operativnih in korporativnih ekipah. MSD deluje v regijah po vsem svetu, njegove karierne priložnosti pa odražajo osredotočenost na raziskave, sodelovanje, vključevanje in odgovoren napredek na področju globalnega zdravja.

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Delovna mesta v podjetju

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

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.

USZdružene države AmerikeNJNew JerseyPAPensilvanija
231.900 $ – 365.000 $ / leto
HibridnoPolni delovni časVodjaZahtevani Jezik: angleščinaSkladnost

Opis

  • Advise Global Clinical Development and Value & Implementation stakeholders worldwide on compliance matters.
  • Join the Value & Implementation Extended Leadership Team and serve as the compliance contact for its organizational leader.
  • Set strategic direction for oversight, data monitoring, analysis, and risk-based recommendations.
  • Brief senior management on compliance matters and external developments that affect internal compliance needs.
  • Advise Value & Implementation, Human Health stakeholders, and business operations on inherent risks.
  • Promote compliant business practices through policy development, compliance communications, and corrective actions.
  • Work with the research division on its Compliance Monitoring Plan to identify and address potential risks.
  • Support due diligence for later-stage business development and integration of completed acquisitions.
  • Coordinate with the Ethics & Compliance Office and International Legal and Compliance on headquarters-led and cross-regional practices.
  • Lead and develop a three-person team based in the United States and Europe.
  • Develop strong teams and talent across the compliance organization.

Zahteve

  • Bachelor’s degree required.
  • At least 15 years of experience, with knowledge of laws, regulations, and policies governing pharmaceutical business practices, especially medical affairs.
  • Experience with advertising and promotion regulations, the Anti-Kickback Statute, and the Foreign Corrupt Practices Act.
  • Experience advising clients and influencing decision-makers, including senior leaders, on legal and compliance matters in life sciences.
  • Strong analytical ability to identify compliance risks and develop mitigation strategies.
  • Sound judgment, disciplined decision-making, emotional intelligence, and an effective advisory style.
  • Strong written and verbal communication and presentation skills.
  • Willingness to travel internationally as needed.
  • Ability to build collaborative relationships across functions, divisions, and regions.
  • Familiarity with research and human health organizations and their activities.
  • Experience developing or implementing written policies and guidance.
  • Experience leading and developing teams, or a strong interest in people management.
  • An advanced degree in science, business, or policy is preferred.
  • A JD from a US-accredited law school or an equivalent degree from outside the United States is strongly preferred.
  • Required skills include compliance program development, compliance reporting, cross-cultural awareness, attention to detail, ethical compliance, sound judgment, leadership, metrics analysis, people management, policy implementation, regulatory compliance audits, regulatory reporting, stakeholder management, technical documentation management, and training and development.

Ugodnosti

  • Annual bonus and long-term incentive, where applicable.
  • Medical, dental, vision, and other insurance coverage for employees and their families.
  • Retirement benefits, including a 401(k).
  • Paid holidays.
  • Vacation leave.
  • Compassionate leave and sick days.
  • Hybrid work arrangement.

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