Investigator Contract Lead 2

Pfizer; Tadworth; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading company in the biopharmaceutical industry seeks an Investigator Contracts Lead to oversee complex contract negotiations and budget management for clinical trials. This hybrid role requires strong expertise in clinical development operations and the ability to navigate challenges in a high-stakes environment. Join Pfizer to contribute to groundbreaking solutions that enhance the patient experience and drive innovations in healthcare.

Benefits

Flexible workplace culture

Diversity and inclusion initiatives

Disability confident employer

Qualifications

• Strong experience in clinical development operations or clinical trial outsourcing.
• Significant experience with clinical study budgets and contracting negotiation.
• Ability to plan and mitigate risks to site contacting timelines.

Responsibilities

• Manage budget and contract negotiations for clinical investigator sites.
• Develop contracts in collaboration with legal and financial teams.
• Lead relationships with investigational sites and oversee the global site budget process.

Skills

Communication

Problem Solving

Negotiation

Education

Bachelor's degree or equivalent

Master's degree (preferred)

Juris Doctorate or equivalent (preferred)

Job description

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Investigator Contracts Lead is responsible for direct site-facing contract and budget negotiations through 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 through start-up. This role may also act as a single point of contact for studies with high priority or complex or unique contracting structures and strategies and is expected to be able to plan and solve for this situations with minimum oversight.

JOB RESPONSIBILITIES

• Exercise independent judgement and decision making in areas of site contracting with moderate supervision.
• Effective management of contract and budget escalations from FSP / pCRO ICL with limited consultation.
• Make appropriate decisions, with limited oversight while balancing the risks for Pfizer in making budget and contractual choices against the impacts to Pfizer clinical trial timelines.
• Problem solving for site contracting issues of moderate complexity. This includes suggesting and implementing unique solutions, as needed, to achieve study goals
• Follow GPD 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 other ICL, pCRO and FSP negotiators in achieving study goals with moderate support from site contracting team leads. 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 advanced knowledge of the principles, concepts and theories in site contracting and budgets.
• 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 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:

• Strong experience in clinical development operations or clinical trial outsourcing and a bachelor’s degree or equivalent.
• Significant 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:

• Strong experience in clinical development operations or clinical trial outsourcing with a master’s degree.
• Limited 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

Work Location Assignment:Hybrid

Purpose

Breakthroughs that change patients' lives... At Pfizer we are apatient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.

One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.

Flexibility

We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self.Let’s start the conversation!

We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer iscommitted to celebratingthis,in all itsforms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.

DisAbility Confident

We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!

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