Medical Director

Scorpion Therapeutics; California (MO); On-site; USD 295,000 - 339,000; Full time

Job summary

Revolution Medicines’ targeted RAS inhibitors in oncology seeks a Medical Director to oversee clinical data integrity and support regulatory submissions. This role focuses on ensuring data accuracy, quality, and timely reporting across programs.

You will lead cross-functional teams in data cleaning, conduct clinical data reviews, and prepare dossiers for NDA/BLA/MAA submissions. Mentorship of clinical teams and collaboration with Regulatory Affairs, Data Management, and Medical Writing are

Qualifications

• MD (or equivalent) with oncology board certification and 5+ years in clinical development
• Experience NDA/BLA regulatory submissions
• GxP, ICH, FDA, EMA guidelines knowledge
• Excellent communication skills

Responsibilities

• Oversee clinical data review
• Ensure compliance with GxP standards
• Lead cross-functional teams in data cleaning and regulatory documentation
• Contribute to strategic clinical development plans
• Collaborate with Regulatory Affairs, Data Management, and Medical Writing to support NDA/BLA/MAA processes; prepare dossiers and responses for health authorities; mentor clinical teams

Skills

Data integrity

Regulatory submissions

Cross-functional leadership

Education

MD / Medical Doctor

Board-certified in Oncology

5+ years in clinical development

Job description

Role: Medical Director supporting clinical development of Revolution Medicines' targeted RAS inhibitors in oncology, focusing on data integrity and regulatory submissions.

Responsibilities:

• oversee clinical data review
• ensure compliance with GxP standards
• lead cross-functional teams in data cleaning and regulatory documentation
• contribute to strategic clinical development plans
• Collaborate with Regulatory Affairs, Data Management, and Medical Writing to support NDA/BLA/MAA processes; prepare dossiers and responses for health authorities; and mentor clinical teams

Requirements:

• MD (or equivalent), board-certified in Oncology, with 5+ years in clinical development, preferably in solid tumors or GI malignancies
• experience with NDA/BLA data review and regulatory submissions
• strong knowledge of GCP, ICH, FDA, EMA guidelines
• excellent communication skills

Preferred: experience with regulatory interactions (e.g., NDA, BLA, Breakthrough Therapy Designation), leading major submissions, and engaging with health authorities and KOLs.

High-Value: Oncology, RAS pathway, targeted therapies, clinical-stage molecules, regulatory dossier preparation, cross-functional leadership, and global regulatory coordination.

Work setup: onsite in Redwood City, CA, with a salary range of $295K-$339K USD.