GSK
Senior Director Team Lead, Therapeutic Area Quality (GCP / Clinical Quality)
$210K–$349K
USA - Pennsylvania - Pennsylvania Central +5 · Hybrid (Remote & On-site) · Director · Full-time · Posted Oct 13, 2026
- Location
- USA - Pennsylvania - Pennsylvania Central
Canada - Ontario - Mississauga
UK - London
USA - North Carolina - Research Triangle Park
USA - Pennsylvania - Upper Providence
Waltham - Experience
- Minimum 3 years of supervisory/management experience; pharmaceutical industry and/or clinical quality assurance experience required, with no duration specified.
- Education
- Bachelor's degree or equivalent in a scientific or quality-related field, or equivalent combination of education, training and experience.
About the job
Leads a global team of Quality Business Partners providing independent GCP oversight across clinical development, shaping quality strategy and ensuring inspection and submission readiness.
What you'll do
- Set and adapt quality strategy and processes; drive improvements informed by risks, audits, inspections, trends, metrics, and root-cause analysis.
- Lead GCP quality support for development projects, including Quality by Design implementation and health authority inspection preparation, execution, and closeout.
- Develop and manage team talent and performance, and communicate critical quality risks to business partners and leadership.
What they ask for
- Bachelor's degree or equivalent in a scientific or quality-related field, or equivalent combination of education, training and experience.
- Demonstrated expertise in GCP and clinical trial quality oversight; pharmaceutical industry and/or clinical quality assurance experience.
- At least 3 years of supervisory/management experience leading a global quality team in an international environment.
- Knowledge of quality assurance, risk management, Quality by Design, GLP, pharmacovigilance/drug safety, and regulatory requirements; experience with Veeva QMS, CTMS and related clinical quality documentation systems.
Nice to have
- Extensive experience supporting regulatory authority GCP inspections.
- Experience with AI/ML and data analytics; broad knowledge of risk-based quality management and root-cause analysis.
Pay
$209,550 to $349,250 USD (annual base salary); CAD0 to CAD0 CAD (annual compensation)
Tools
Veeva QMS, CTMS, AI/ML
AI focus
AI/ML experience is a preferred qualification; the role's core work is GCP clinical quality oversight, not AI development.
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