Qualifications

• Trained MD or MD-Ph.D. degree.
• 7+ years of experience in drug development or as a clinical investigator/physician-scientist; oncology experience preferred.
• Patient-focused with a commitment to improving patient lives.
• Successful team collaboration across multiple functions.
• Proven record of accomplishment and ability to meet deadlines in high-performance settings.
• Motivated to work in fast-paced, high-accountability environments; strong interpersonal skills.
• Strong written and oral communication skills, particularly in presentations.

Responsibilities

• Serve as trial medical lead/medical monitor for clinical studies, guiding study oversight and management plans.
• Cultivate relationships with clinical investigators and thought leaders to enhance trial execution and opportunities.
• Ensure compliance with ethical and regulatory guidelines for clinical studies.
• Lead investigator meetings and site initiation visits to foster effective study launches.
• Provide expert support for clinical trial documents and regulatory submissions.
• Contribute to the writing and preparation of key scientific manuscripts and presentations.
• Translate research findings into actionable clinical development opportunities.

Benefits

• Comprehensive healthcare coverage.
• Opportunities for professional development and continuous learning.
• Flexible work arrangements to maintain work-life balance.
• Collaborative and innovative work culture.
• Engagement in meaningful work that directly impacts patient outcomes.