Process & Standards Lead

Pfizer • La Jolla, PA

3d • Onsite

About The Position

At Pfizer, we foster evidence-based medical decision support that contributes to better health and treatment outcomes. Our frameworks ensure scientific soundness and deliver unbiased, medically essential expertise. By addressing data gaps, we strengthen our mission to empower healthcare decisions and ensure the safe and proper use of medicines for patients. Aligning efforts with scientific rigor and clinical necessity, your role will facilitate improved health outcomes and support the informed, effective use of medical treatments. In this role, you will: Lead and manage highly complex projects, developing and executing mid-term plans that drive impactful results. Oversee clinical studies, ensuring strict adherence to established timelines, budgets, and scope of work. Act as an advisor, leveraging relationships to fulfill the needs of Global Business Units. Make informed decisions in complex situations, identifying innovative solutions and recommending appropriate courses of action. Build and utilize relationships throughout the organization to achieve divisional goals. Independently initiate and manage projects, tapping into the knowledge of others and making sound judgments in complicated decision-making processes. Serve as the main point of contact for study teams during the site feasibility process. Work closely with therapeutic business units to drive the execution of Site Intelligence and Feasibility initiatives. Oversee the development and implementation of global publication plans, ensuring compliance with Pfizer’s publication policies and procedures. Review and evaluate the work of colleagues, using foresight and judgment based on extensive experience and knowledge within the unit.

Requirements

• BA/BS with at least 8 years of experience or MBA/MS with at least 7 years of experience or PhD/JD with at least 5 years of experience or MD/DVM with at least 4 years of experience
• Proven aptitude for analyzing and solving problems pragmatically
• Proficient in managing multiple projects simultaneously
• Ability to prioritize tasks effectively
• Flexibility and adaptability to work autonomously or collaboratively in a matrix environment
• Exceptional verbal and written communication skills
• Expertise in project management and proficiency in Microsoft Office Suite

Nice To Haves

• In-depth experience in pharmaceutical or clinical trial settings
• Mastery in using publications management tools
• Expert knowledge in developing and managing medical publications from clinical trials
• Strong analytical and strategic thinking skills
• Ability to drive innovative solutions and enhance organizational efficiency
• Advanced problem-solving abilities and dedication to achieving new milestones
• Effective stakeholder management and influence within matrix environments
• Outstanding leadership and mentoring abilities
• Adaptability and resilience in dynamic business environments
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity.
• Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
• Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.

Responsibilities

• Lead and manage highly complex projects, developing and executing mid-term plans that drive impactful results.
• Oversee clinical studies, ensuring strict adherence to established timelines, budgets, and scope of work.
• Act as an advisor, leveraging relationships to fulfill the needs of Global Business Units.
• Make informed decisions in complex situations, identifying innovative solutions and recommending appropriate courses of action.
• Build and utilize relationships throughout the organization to achieve divisional goals.
• Independently initiate and manage projects, tapping into the knowledge of others and making sound judgments in complicated decision-making processes.
• Serve as the main point of contact for study teams during the site feasibility process.
• Work closely with therapeutic business units to drive the execution of Site Intelligence and Feasibility initiatives.
• Oversee the development and implementation of global publication plans, ensuring compliance with Pfizer’s publication policies and procedures.
• Review and evaluate the work of colleagues, using foresight and judgment based on extensive experience and knowledge within the unit.

Benefits

• 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
• health benefits to include medical, prescription drug, dental and vision coverage

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level