Job Summary
Job Summary: The Asset Quality Lead, GCP Inspections (AQL) is responsible for driving GCP Quality by maintaining ‘quality’ line-of sight for assigned clinical trial programs/protocols. The AQL 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
* Monitor submission risk and flag major risks for Category Quality Head review and other key stakeholders for review
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
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
* Coordinate GCP inspection support activities with IMQA, including 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 incorporation into study level risk planning
* Provide strategic input to risk-based quality approaches
* Where appropriate, perform Quality Integration activities including representing quality functional lines at integration/workshops, facilitating GCP Quality Integration Workstreams, and developing quality project plans for GCP business deal activities
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
Oncology Experience Strongly Preferred
* Advanced clinical trials experience, especially operational processes and/or systems
* Strong interpersonal skills, ability to influence, engage leaders and maintain excellent working relationships across lines in a matrix organization
* Experience of working on global initiatives or project teams
* Appreciation of diverse regulatory needs of various sites and countries
* Extensive knowledge of regulations to assess GCP situations and coordinate resolution across partner lines
* Excellent knowledge of Pfizer SOPs and quality management processes
* Extensive Quality related experience including working knowledge in: Quality and compliance management, QC; Root Cause Analysis; Metrics development and utilization; Audit and Inspection conduct; CAPA development and response process; Inspection Readiness; Project/initiative coordination and management; Spotfire and Excel skills
Organizational Relationships
Partners with key stakeholders such as Clinical Development & Operations, RQA, Data Sciences and Analytics, Global Clinical Supply and BPOs. Candidate demonstrates a breadth of leadership experiences and capabilities including the ability to influence and collaborate with peers, develop and coach others, and oversee the work of other colleagues to achieve meaningful outcomes and business impact.
Work Location
Work Location Assignment: Hybrid
Compensation and Benefits
The annual base salary for this position ranges from $162,900.00 to $271,500.00. This position is eligible for participation in Pfizer’s Global Performance Plan with a target bonus of 20.0% of base salary and eligibility for long-term incentive programs. Benefits include a 401(k) with Pfizer matching, retirement contributions, paid vacation, holidays, parental leave, medical/dental/vision coverage, and more. Salary specifics for Tampa, FL: $146,600.00 to $244,400.00. Relocation assistance may be available based on business needs and eligibility.
Sunshine Act, EEO & Employment Eligibility statements are included as required.
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