Director, Oncology Clinical Science — Hybrid Role

GSK; Upper Providence (Delaware County); Hybride; USD 190 000 - 316 000; Plein temps

Avantages offerts par ce poste

Annual bonus

Long-term incentive program

Health care

Retirement benefits

Paid holidays

Résumé du poste

GSK is seeking a Director, Clinical Scientist – Oncology Clinical Development, to lead science across study-level activities and collaborate with cross-functional teams. The role emphasizes rigorous data interpretation, robust study design, and strategic input to asset-level decisions while maintaining scientific quality across documents.

You will be part of a hybrid, on-site at key locations with flexible remote days, contributing to advancing cancer therapies through innovative science and

Qualifications

• Bachelor’s degree in life sciences or related scientific discipline.
• Experience in pharmaceutical/biotechnology clinical development.
• Experience with GCP/ICH and regulatory guidelines.

Responsabilités

• Provide scientific leadership across study-level activities within CDL direction.
• Contribute to protocol development, study design, data review, and interpretation.
• Collaborate with Clinical Matrix Team to align timelines and deliverables.
• Ensure quality of protocols, IBs, CSRs, and regulatory submissions.
• Analyze data to generate insights on safety, efficacy, and populations.
• Engage with investigators and external experts to support studies.

Connaissances

Analytical Thinking

Clinical Research

Clinical Trial Designs

Leadership

Strategic Thinking

Communication

Decision Making

Fostering Collaboration

Matrix Leadership

Risk Management

Formation

Bachelor’s degree in life sciences

Description du poste

GSK is seeking a Director, Clinical Scientist – Oncology Clinical Development, to lead science across study-level activities and collaborate with cross-functional teams. The role emphasizes rigorous data interpretation, robust study design, and strategic input to asset-level decisions while maintaining scientific quality across documents.

You will be part of a hybrid, on-site at key locations with flexible remote days, contributing to advancing cancer therapies through innovative science and