Senior Director, Clinical Development

Scorpion Therapeutics; California (MO); On-site; USD 210,000 - 350,000; Full time

Benefits offered by this job

Competitive salary

Benefits

Job summary

Revolution Medicines seeks a Senior Director, Clinical Science to drive clinical strategy across its oncology programs targeting RAS mutations. You will lead trial design, oversee data review, and collaborate with cross-functional teams to advance late-stage development.

The role involves mentoring teams, coordinating with regulatory agencies, and shaping the clinical development plan. Onsite work is expected at Redwood City, CA, with a competitive compensation and benefits package.

Qualifications

• PhD, PharmD, or equivalent.
• 10+ years in clinical development or related pharma R&D, with extensive expertise in oncology, particularly RAS pathway mutations
• Strong knowledge of GCP, ICH, FDA, EMA regulations
• Experience in trial design, protocol writing, and cross-functional coordination
• Proven regulatory engagement skills

Responsibilities

• Lead clinical science strategies and documentation, oversee trial design and execution, and manage clinical data review and reporting
• Represent the clinical development plan across teams
• Mentor teams and collaborate with regulatory and scientific stakeholders

Skills

Clinical development leadership

Oncology expertise (RAS mutations)

Regulatory engagement

Education

PhD/PharmD or equivalent

Job description

Role

Senior Director, Clinical Science, supporting Revolution Medicines' clinical-stage oncology programs targeting RAS mutations.

Responsibilities

• lead clinical science strategies and documentation, oversee trial design and execution, and manage clinical data review and reporting
• represent the clinical development plan across teams
• mentor teams and collaborate with regulatory and scientific stakeholders

Requirements

• PhD, PharmD, or equivalent
• 10+ years in clinical development or related pharma R&D, with extensive expertise in oncology, particularly RAS pathway mutations
• strong knowledge of GCP, ICH, FDA, EMA regulations
• experience in trial design, protocol writing, and cross-functional coordination
• proven regulatory engagement skills

Preferred

• contributions to regulatory submissions
• experience with major health authority interactions
• leadership in clinical development strategy
• process improvements

High-Value

• oncology
• RAS mutations
• G12C/G12D/G12V inhibitors
• late-stage clinical development
• regulatory submission experience
• cross-functional leadership

Work Setup

likely onsite at Redwood City, CA, with competitive salary and benefits.