Asset Quality Lead, Director

Job Summary
The Asset Quality Lead (AQL) is responsible for driving GCP Quality by maintaining 'quality' line-of sight for assigned clinical trial programs/protocols. With this focus, the AQL role brings deep knowledge of GCP quality and risk management principles to asset and study teams. In partnership with the cross functional study team and functional lines in Clinical Development & Operations, the AQL will ensure program and study level quality oversight, drive quality risk management and inspection readiness activities and will be instrumental in ensuring that asset and study level information is appropriately incorporated within the GCP QMS. The AQL is the point person to the cross functional study team and other relevant stakeholders for quality risk management, quality issues management and general GCP guidance.
JOB RESPONSIBILITIES
Asset-Level Quality Oversight

• Ensure clinical development plan strategy and asset-level risks are incorporated into study and asset level risk management and oversight to support GCP Compliance
• Strategically, utilize quality measures/data to monitor asset/study quality and identify potential risks, quality trends, and support state of quality reporting
• Communicate key quality information across study teams and serve as GCP quality expert to study teams

Study-Level Risk Management Plan Development and Oversight

• Oversee study-level quality risk management activities, including driving Study Risk Profile development/maintenance and QTL implementation by ensuring that quality metrics are monitored and that quality deviations are identified and addressed in a timely and appropriate manner
• Develop and present quality point of view at governance and portfolio related meetings
• Monitor submission risk and flag major risks for Category Quality Head review and other key stakeholders for review

Inspection Readiness, Preparation and Support

• Provide Study Team Inspection Readiness(IR) guidance and support to asset teams and pivotal study teams that have a high likelihood of regulatory inspection; lead teams through pre-submission IR deep dive and storyboards
• Develop and maintain inspection readiness tools and processes  In conjunction with IMQA, coordinate business line GCP inspection support activities including but not limited to requests for dossiers, pre-inspection requests, during inspections and through the development of written responses to findings.

Business Development

• GCP quality representative of the PRD due diligence team for business development opportunities.
• GCP quality representative on integration teams responsible for the identification of key quality risks and proposed mitigations and incorporate into study level risk planning.
• Provide strategic input to risk-based quality approaches
• Where appropriate, perform Quality Integration activities including but not limited to: representing quality functional lines at integration workshops or operational workshops, facilitating GCP Quality Integration Workstreams, and developing quality project plans for GCP business deal activities (e.g., integration operations)

Escalation, Communication, and Governance

• Develop and present quality related information at relevant governance and/or operational meetings
• Advise asset/study team on appropriate escalation pathways for quality concerns
• Communicate key quality information (e.g. inspection/audit learnings) across asset/study and serve as asset quality expert
• Lead asset level/study level quality risk planning activities

BASIC QUALIFICATIONS
A scientific or technical degree is preferred. In general, candidates for this job would have the following levels of experience:
BS: 10+ years or equivalent
MS/MBA: 7+ years or equivalent
Ability to build strong network/knowledge/relationships with internal/external stakeholders
Strong, advanced knowledge, experience and expertise in ICH GCP, clinical trial development, and operational GCP quality management disciplines such as, quality and compliance assessments, quality assurance, CAPA management, deviation management, root cause analysis, audit and regulatory inspection process, and/or inspection readiness.
Familiarity with the relevant key therapeutic area(s)
PREFERRED QUALIFICATIONS
Advanced clinical trials experience, especially operational processes and/or systems.
Strong interpersonal skills, ability to influence, engage leaders and ability to establish and maintain excellent working relationships across lines in a matrix organization
Experience of working on global initiatives or project teams.
Appreciation of diverse needs of different regulatory requirements of various sites and countries
Extensive knowledge of regulations in order to assess GCP situations and to coordinate resolution activities across partner lines
Extensive Quality related experience including working knowledge in areas of:

• Quality and compliance management, QC
• Root Cause Analysis
• Metrics development and utilization
• CAPA development and response process
• Audit and Inspection conduct
• Inspection Readiness
• Project/initiative coordination and management skills

Spotfire and Excel skills/experience
Excellent knowledge of Pfizer SOPs and quality management processes
#LI-PFE
The annual base salary for this position ranges from $162,900.00 to $271,500.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 20.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include 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, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation assistance may be available based on business needs and/or eligibility.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
Sunshine Act
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EEO & 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, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
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Quality Assurance and Control