Clinical Director Sr Medical Director

Scorpion Therapeutics; Cambridge (MA); On-site; USD 260,000 - 380,000; Full time

Job summary

Scorpion Therapeutics is seeking a Senior Medical Director in clinical development for the GU portfolio to lead scientific strategy, oversee trial design, and ensure ethical and regulatory standards across programs.

You will supervise medical monitoring activities, oversee investigator interactions, serve as clinical contact with regulators and ethics committees, and contribute to clinical and regulatory documentation with cross-functional leadership in late-phase development.

Qualifications

• MD/DO/MBBS/MBChB with 4+ years in biopharma clinical R&D.
• Licensed to prescribe medicines for at least 2 years.
• Board certification or eligibility in oncology preferred, especially breast cancer, with late-phase trial experience.

Responsibilities

• Oversee medical monitoring activities (eligibility, data review, safety).
• Lead investigator interactions.
• Serve as clinical contact with regulators and ethics committees.
• Contribute to clinical and regulatory documentation.
• Provide strategic clinical insights.

Skills

Regulatory engagement

Cross-functional leadership

Investigator interactions

Clinical data review

Strategic clinical insights

Education

MD/DO/MBBS/MBChB

Job description

Role: Senior Medical Director in clinical development for the GU portfolio, focusing on supporting clinical trials and leading subteams to meet scientific, ethical, and regulatory standards.

Responsibilities

• oversee medical monitoring activities (eligibility, data review, safety)
• lead investigator interactions
• serve as clinical contact with regulators and ethics committees
• contribute to clinical and regulatory documentation
• provide strategic clinical insights

Requirements

• MD/DO/MBBS/MBChB with 4+ years in biopharma clinical R&D
• licensed to prescribe medicines for at least 2 years

Preferred

• board certification or eligibility in oncology, especially breast cancer, with late-phase clinical trial experience

High-value details

• oncology therapeutic area
• late-phase development
• regulatory engagement
• GxP compliance
• cross-functional leadership
• external representation

Work setup

not specified.