Site Contracts Template Specialist, Clinical Development
hace 7 días
Job Summary
The Site Contracts Template Specialist plays a crucial role in identifying and prioritizing opportunities to maintain an appropriate inventory of site contract templates. This position requires revising global, country, and site-specific templates to align with changing external and internal requirements.
Key Responsibilities
- Act as a divisional subject matter expert for country and site template updates for Pfizer Research & Development and Pfizer Oncology Divisions.
- Maintain strong business awareness, evaluating current and future policies, practices, trends, technology, and information affecting Investigative Site Contracting.
- Recommend changes to templates based on knowledge and experience.
- Collaborate with Pfizer Legal to ensure Investigative Site contracting templates are maintained and continuously improved.
- Manage the introduction of revised templates by gaining approvals and efficiently communicating changes to 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.
- Negotiate or oversee site contracting professionals in negotiation and execution of assigned contracts.
Requirements
- 7+ years of experience in clinical development operations or clinical trial outsourcing with a bachelor's degree or equivalent.
- Experience 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 are 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 Clinical Trial Agreements with clinical trial sites in a global operation.
Benefits
Pfizer offers comprehensive and generous benefits and programs to help our colleagues lead healthy lives and support each of life's moments. Benefits include 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.
Equal Opportunity Employer
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or expression, national origin, disability, or veteran status.
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