Senior Associate Director, Oncology Diagnostics Planning

GSK; Upper Providence (Delaware County); On-site; USD 120,000 - 160,000; Full time

Job summary

GSK's Diagnostics Planning Team within Oncology Translational Medicine seeks a Dx Planning Lead to overseeDx development activities, coordinate internal and external collaborations, and drive documentation for regulatory submissions. The role requires leading cross-functional teams and ensuring milestones, timelines, and budgets are met.

Ideal candidates have 7+ years in project/program management in diagnostics/pharma, plus familiarity with drug discovery, clinical trials, and regulatory

Qualifications

• Bachelor's degree in biological sciences or related discipline.
• 7+ years of project or program management experience in diagnostics/pharma/biotech.
• Experience managing clinical biomarker or diagnostic development programs.
• Knowledge of drug discovery, clinical trial design and regulatory concepts.

Responsibilities

• Lead cross-functional project teams across Clinical Development, Data Management, QA, Regulatory, and Finance.
• Represent GSK to external partners to ensure scope, cost, quality, and timeline milestones.
• Plan, track, and communicate timelines, milestones, and goals to teams and stakeholders.
• Monitor budgets, milestones, payments, and invoices for diagnostics projects.
• Organize internal and external meetings; document discussions and actions for follow-up.
• Contribute to strategic planning aligning with Oncology Translational Medicine goals.
• Manage multiple projects concurrently with accountability and urgency.

Skills

Project management

Cross-functional leadership

Biological sciences

Budget management

Risk management

Education

Bachelor's degree in biological sciences or related discipline

Tools

MS Project

Power BI

MS Teams

SharePoint

Job description

GSK's Diagnostics Planning Team within Oncology Translational Medicine seeks a Dx Planning Lead to overseeDx development activities, coordinate internal and external collaborations, and drive documentation for regulatory submissions. The role requires leading cross-functional teams and ensuring milestones, timelines, and budgets are met.

Ideal candidates have 7+ years in project/program management in diagnostics/pharma, plus familiarity with drug discovery, clinical trials, and regulatory