Site Contracts Template Specialist

hace 2 días

Madrid, Madrid, España Pfizer A tiempo completo

Job Summary

The Site Contracts Template Specialist is a critical role within Pfizer's Clinical Development team, responsible for identifying and prioritizing opportunities to maintain and improve site contract templates. This position requires a strong understanding of the Biopharmaceutical industry and the ability to draft, review, and communicate changes to site contract templates.

Key Responsibilities

  • Develop and maintain a deep understanding of Pfizer's clinical development operations and the Biopharmaceutical industry.
  • Collaborate with Pfizer Legal to ensure Investigative Site contracting templates are maintained and continuously improved.
  • Recommend changes to templates based on knowledge and experience.
  • Manage the introduction of revised templates by gaining appropriate approvals and efficiently communicating changes to all stakeholders.
  • Update contract template guidance and repository to support contract template changes.
  • Ensure training is delivered and documented to site contracting professionals around Investigative Site Contracting policies, templates, and standards.

Requirements

  • 7+ years of experience in clinical development operations or clinical trial outsourcing and a bachelor's degree or equivalent.
  • Experience in working with limited supervision to achieve business goals.
  • Experience with contracts and negotiation principles, practices, processes, and activities is essential.
  • Balance of general business, compliance, finance, legal, and drug development or legal/compliance experience in a regulated industry is essential.
  • Strong and precise communications and presentation skills essential to success.
  • Record of achievement and delivery against personal goals.
  • Demonstrated ability to lead by influence rather than positional power to accomplish critical deliverables.
  • Demonstrated success in working in a highly matrix-based organization.

Preferred Qualifications

  • 5+ years of experience in clinical development operations or clinical trial outsourcing with a master's degree.
  • 2+ years of experience in clinical development operations or clinical trial outsourcing with a Juris Doctorate (or equivalent).
  • Expertise in drafting and negotiating of Clinical Trial Agreements with clinical trial sites in a global operation.

Benefits

Pfizer offers a comprehensive and generous benefits package, including a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday, and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental, and vision coverage.

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