Senior Manager, Corporate Audit

Posted 3 Hours Ago
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Hiring Remotely in Ringsend, Ulster, IRL
Remote
Senior level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Leads independent Good Clinical Practice audits and risk oversight activities for clinical development. Plans audit scopes, evaluates controls and regulatory compliance, analyzes data, identifies risks, communicates findings, and recommends corrective actions. Partners with business leaders and Corporate Audit teams to improve oversight processes, manage projects, and address compliance gaps. Requires extensive GCP operational and quality compliance experience, strong analytical and communication skills, and up to 30% domestic and international travel.
Summary Generated by Built In
Role Summary
The Senior Manager - GCP Auditor is responsible for planning, leading and conducting Good Clinical Practice (GCP) independent audits and risk oversight activities. These audits/activities provide an independent assessment of the design and operating effectiveness of controls and compliance with appropriate GCP regulations, industry standards, internal policies and procedures and good business practices. Additionally, this individual interfaces with business representatives and makes recommendations on oversight approaches for risk mitigation.
Role Responsibilities
Audits
Provides fact-based input into the risk assessment of audit targets and leads/conducts scheduled audits in accordance with Corporate Audit processes. Analyzes risk information applying critical thinking and demonstrates high level of learning agility. Adapts audit methodologies across a broad set of risks to develop customized audit plans. Collaborates with the Audit Director and the Analytics and Innovation team to develop an audit plan, including data analytics where applicable, to support controls testing as appropriate. Manages the appropriate prioritization of work to execute an effective work plan for audit/project work and keeps Audit Director regularly apprised of status and issues. Analyzes large data sets to identify potential risks and discrepancies. Provides clear and concise verbal and written communication of audit findings and to senior site and division management, including practical recommendations to address identified risks, requiring strong negotiation and influence skills. Documents audit work and prepares formal written reports setting forth recommendations for local, division and corporate management to strengthen and improve operations. Conducts or supports other oversight activities (e.g., Assessments, compliance investigations) as assigned. Identifies ways to improve audit processes to ensure appropriate assessments of controls in an evolving business model.
Analysis
1. Recommends approaches for oversight activities to mitigate risks across the assigned business line.
2. Identifies ways to improve oversight and assessment processes.
Relationship Management
1. Works within functional area to ensure consistency in approach and to minimize gaps and redundancies in activities.
2. Cultivates strong relationships within Corporate Audit to achieve an effective oversight program.
3. Uses compliance and business intelligence to forge relationships critical to a comprehensive oversight program.
Other Activities
1. Maintains high level of awareness of changing needs of the business, industry trends, competitive activities, and regulatory environment.
2. Takes on special projects at the request of management.
3. Serves on Corporate Audit departmental committees/teams, as necessary.
4. Assists in the development/updating of Corporate Audit departmental standard operating and administrative procedures.
5. Serves as a resource on GCP compliance matters for their area of subject matter expertise.
Skills, Qualifications and Experience
  • Bachelor's degree, preferably in an area such as Biology, Chemistry, Nursing, Medical Technology, Pharmacy, or health. Advanced degree preferred.
  • Ten or more years of relevant GCP International operational experience in clinical development required.
  • Five years' experience in GCP quality related compliance discipline.
  • A thorough understanding and extensive knowledge of ICH GCP and applicable global & local regulations/guidance for clinical development.
  • Previous experience in GCP risk assessment and/or analysis strongly preferred.
  • Demonstrated ability to apply knowledge of regulations, policies and standards to assess compliance.
  • Ability to assess systems and processes in a highly systematic manner and make conclusions based on sound judgment and experience to identify gaps and potential risk.
  • Strong analytical skills with the ability to digest and interpret complex data.
  • Ability to rapidly comprehend Pfizer organization and agility in maneuvering across the organization.
  • Experience working in dynamic complex business models (e.g., outsourcing and partnerships)
  • Strong strategic thinking capability and decision-making skills
  • Demonstrated excellent project management skills; able to manage multiple projects and demanding timelines
  • Proven leadership skills
  • Excellent written and verbal communication and presentation skills to convey audit findings and recommendations effectively.
  • Excellent interpersonal and negotiation skills, with a demonstrated ability to effectively interact with clients, influence others, identify compliance gaps, and communicate pathways for corrective/preventative actions.
  • Attention to detail and the ability to work independently as well as collaboratively within a team.
  • Ability to create a strong collaborative environment working with all levels of management.
  • A self-starter who holds themselves and others accountable.
  • Ability to travel (both domestic and international) up to 30%.

Travel requirements 30%
The closing date for applications is September 20th.
Make a difference today! All suitable candidates should apply through the link with CV provided. We are looking forward to hearing from you!
In order to be considered for this position you need to be legally eligible to work in the EU.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Due to the high volume of applications we will be contacting successful candidates only.
Additional Information
  • In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland.
  • Please note there is no relocation support available for this position

How to apply
  • Make a difference today, all suitable candidates should apply with CV below. We are looking forward to hearing from you!

Purpose
Breakthroughs that change patients' lives... At Pfizer we are a patient 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.
Digital Transformation Strategy
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.
Equal Employment Opportunity
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms - 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 Inclusion
Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [email protected]. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Finance & Accounting

Skills Required

  • Bachelor's degree, preferably in biology, chemistry, nursing, medical technology, pharmacy, or health
  • Ten or more years of relevant international GCP operational experience in clinical development
  • Five years of experience in GCP quality-related compliance
  • Thorough understanding of ICH GCP and applicable global and local clinical development regulations and guidance
  • Ability to assess compliance using regulations, policies, and standards
  • Strong analytical skills and ability to interpret complex data
  • Experience working in dynamic, complex business models, including outsourcing and partnerships
  • Strong strategic thinking and decision-making skills
  • Excellent project management skills and ability to manage multiple projects and demanding timelines
  • Proven leadership skills
  • Excellent written, verbal, and presentation skills
  • Excellent interpersonal and negotiation skills
  • Ability to work independently and collaboratively
  • Ability to travel domestically and internationally up to 30%
  • Advanced degree
  • Previous GCP risk assessment or analysis experience

What the Team is Saying

Daniel
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Esteban
Pfizer

Pfizer Compensation & Benefits Highlights

  • Healthcare Strength Health coverage is described as comprehensive, spanning medical, dental, vision, and robust mental‑health benefits, with eligible Pfizer medications available at no cost in U.S. plans. Family‑building support and transgender‑inclusive care are explicitly included, alongside wellbeing resources such as a reimbursement wallet and telehealth options.
  • Retirement Support Retirement programs feature a 401(k) with company matching plus an additional Retirement Savings Contribution, complemented by company‑subsidized life, short‑term disability, and long‑term disability insurance. Materials also reference subsidized retiree medical coverage for eligible groups.
  • Leave & Time Off Breadth Paid vacation, holidays, personal days, and paid parental and caregiver leave are consistently highlighted in current U.S. summaries and job postings. Options like buying extra vacation days and transition‑back support strengthen the time‑off offering.

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The Company
HQ: New York, NY
121,990 Employees
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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Pfizer Offices

Hybrid Workspace

Employees engage in a combination of remote and on-site work.

Typical time on-site: 2.5 days a week
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