Senior Director Clinical Development, Solid Tumor

Scorpion Therapeutics; United States; Hybrid; USD 180,000 - 280,000; Full time

Job summary

BeOne is seeking a Clinical Development Lead to oversee strategic planning and execution of partnership oncology clinical programs within BeOne's SuperHighway platform. The role requires MD/DO credentials with extensive oncology program experience, and a track record of leading complex, global studies.

You will guide global teams and external partners, author pivotal regulatory documents, and mentor staff while driving high-quality study execution and strategic alignment with regulatory and

Qualifications

• MD or DO with 6+ years in clinical development, including 5+ years in oncology.
• Strong oncology therapeutics expertise and global regulatory alignment.
• Experience leading cross-functional teams and managing vendor and investigator selection.

Responsibilities

• Develop clinical strategies aligned with regulatory and commercial goals.
• Ensure high-quality, compliant study execution.
• Provide scientific and medical guidance for programs.
• Author regulatory and study documents.
• Build investigator networks and mentor team members.
• Monitor study progress, KPIs, and quality across programs.
• Collaborate with global teams and external partners.
• Participate in therapeutic research and competitive analysis.
• Manage issue escalation as needed.

Skills

oncology therapeutics

global compliance

strategic leadership

vendor selection

investigator selection

team management

Education

MD/DO

Job description

Role: Clinical Development Lead overseeing strategic planning and execution of partnership oncology clinical programs within BeOne's SuperHighway platform.

Responsibilities

• develop clinical strategies aligned with regulatory and commercial goals;
• ensure high-quality, compliant study execution;
• provide scientific and medical guidance;
• author key regulatory and study documents;
• build investigator networks;
• mentor team members;
• monitor study progress, KPIs, and quality;
• collaborate across global teams and external partners;
• participate in therapeutic research and competitive analysis;
• and manage issue escalation.

Qualifications

• MD or DO with 6+ years in clinical development, including 5+ years in oncology;
• 10+ years preferred;
• Skills include oncology therapeutics expertise, global compliance knowledge, strategic leadership, vendor and investigator selection, and team management;
• High-value biopharma specifics: oncology (immuno-oncology focus), therapeutic area experience, global regulatory alignment, clinical trial conduct, and cross-functional collaboration.

Work setup: hybrid with up to 20% domestic and international travel.