Investigator Contract Lead I

Investigator Contract Lead I page is loaded## Investigator Contract Lead Ilocations: Brazil - São Paulotime type: Full timeposted on: Posted Todayjob requisition id: **JOB RESPONSIBILITIES*** Exercise good judgment in balancing the risks for Pfizer in making budget and contractual decisions against the impacts to Pfizer clinical trial timelines.* Follow GSSO processes to develop, negotiate, track and execute global clinical study agreements with institutions and investigators participating in sponsored clinical trials.* Work with partners to develop and oversee the global site budget process.* Work with clinical trial sites and directly negotiate cost, business and contractual terms and conditions with investigators/institutions, making changes to contract templates within the Legal division approved parameters.* Lead and develop relationships with key investigational sites and Site Management Organizations across the contracting and budgeting interface.* Lead study level site contracting activities, direct other ICL and act as primary study point of contract for site contracting issues and timelines on assigned studies.* Partner with Legal and other divisions to manage escalations in the site budgeting and contracting space.* Partner with Legal, Finance, pCRO and other divisions to identify and implement areas of improvement in the site contracting space.* Has knowledge of the principles, concepts and theories in applicable business discipline.* Collaborates with invoicing specialists and/or invoice service provider to ensure alignment with Investigative Site contracting and compensation requirements.* Applies acquired job skills and procedures to complete substantive assignments, projects and tasks of moderate scope and complexity in applicable discipline.* Contributes to design, development and implementation of major business initiatives or special projects. Applies technical skills and discipline knowledge to contribute to the achievement of business objectives at GPD or WSR Functional Line level – e.g., WSR Worldwide Safety, WSR Worldwide Regulatory Operations, GPD Clinical Development & Operations, etc.**QUALIFICATIONS / SKILLS****Basic Qualifications:*** 5+ years of experience in clinical development operations or clinical trial outsourcing and a bachelor’s degree.* Experience with clinical study budgets and contracting negotiation principles, practices, processes, and activities.* Balance of general business, compliance, finance, legal, and drug development experience.* Precise communications and presentation skills.* Ability to plan, identify and mitigate risks to site contacting timelines.* 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:*** 2+ years of experience in clinical development operations or clinical trial outsourcing and a US Juris Doctorate or equivalent legal degree.* Experience in drafting and negotiating of Clinical Trial Agreements with clinical trial sites in a global operation.**Other Job Details:*** Primary location: São Paulo - Brazil* Work Location Assignment: On-site 2-3x/week or as needed by the business* Last day to apply for job: September 26, 2025**EEO (Equal Employment Opportunity) & Employment Eligibility**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 gender expression, national origin, or disability.Global ProcurementPfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.
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