Hybrid Global Oncology Regulatory Manager

GSK; Baar; Hybrid; CHF 91,000 - 152,000; Full time

Job summary

GSK is seeking a Global Regulatory Affairs Manager to lead regulatory strategies for oncology assets across regions. You will collaborate with cross-functional teams to shape development plans, submissions, and labeling while ensuring compliance with regulatory requirements.

The role reports to GRL and TA Head, with a patient‑first mindset and a focus on strategic guidance, risk assessment, and timely approvals across multiple markets.

Qualifications

• Minimum: Bachelor’s degree in biological, pharmaceutical or healthcare science.
• Proven experience in drug development process, preferably in regulatory affairs and oncology.
• Knowledge of clinical trial and licensing requirements in at least one major regional/global market.
• Strong written and verbal communication skills for clarity and impact.
• Experience working effectively in matrix teams.

Responsibilities

• Develop and deliver global regulatory strategies for oncology assets.
• Collaborate with cross-functional teams to align plans with development strategies.
• Support regulatory interactions, reviews, and submissions across regions.
• Assess regulatory intelligence to inform strategy and decision-making.
• Ensure compliance with global/regional/local requirements throughout product lifecycle.
• Drive process improvements and strategic changes in regulatory functions.

Skills

Business resilience

Communication

Digital fluency

Matrix leadership

Pharmaceutical regulatory compliance

Regulatory strategies

Resource management

Stakeholder management

Education

Bachelor’s degree in biological, pharmaceutical or healthcare science

Advanced degree (PhD, MD, PharmD)

Job description

GSK is seeking a Global Regulatory Affairs Manager to lead regulatory strategies for oncology assets across regions. You will collaborate with cross-functional teams to shape development plans, submissions, and labeling while ensuring compliance with regulatory requirements.

The role reports to GRL and TA Head, with a patient‑first mindset and a focus on strategic guidance, risk assessment, and timely approvals across multiple markets.