Lead Investigator

1 month ago


Tadworth Surrey, United Kingdom Pfizer Full time

Creating value though site contracting is keeping our products in production and our innovators innovating. The Investigator Contracts Lead is responsible for direct site-facing contract and budget negotiations thought contract execution with assigned clinical investigator sites including initial agreements and amendments and oversight of other contracting professionals on assigned studies. This also includes managing the Per-Subject Cost (PSC) process for assigned studies, managing escalation and resolution for budget and non-legal term issues from other ICL or pCRO and collaborating with other lines to plan site contracting timelines though start-up.

Exercise good judgment in balancing the risks for Pfizer in making budget and contractual decisions against the impacts to Pfizer clinical trial timelines.
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.
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. WSR Worldwide Safety, WSR Worldwide Regulatory Operations, GPD Clinical Development & Operations, etc. ?
It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.

Proven/extensive experience in clinical development operations or clinical trial outsourcing and a bachelor's degree.
* Balance of general business, compliance, finance, legal, and drug development experience.
* Ability to plan, identify and mitigate risks to site contacting timelines.
* Advanced Microsoft Office Suite skills and strong competency with tools.
* Good organizational, negotiation skills and time management capability.
Experience in clinical development operations or clinical trial outsourcing and a US Juris Doctorate or equivalent legal degree.
* 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. WSR Worldwide Safety, WSR Worldwide Regulatory Operations, GPD Clinical Development & Operations, etc.
?
It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.
Proven/extensive experience in clinical development operations or clinical trial outsourcing and a bachelor's degree.
* Balance of general business, compliance, finance, legal, and drug development experience.
* Ability to plan, identify and mitigate risks to site contacting timelines.
* Advanced Microsoft Office Suite skills and strong competency with tools.
* Good organizational, negotiation skills and time management capability.



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