What are the responsibilities and job description for the Clinical Study Lead position at Meet Life Sciences?
Clinical Study Lead (Oncology)
Carlsbad, CA (Hybrid – Onsite 1x/week)
We are partnering with a small, growing biotech developing innovative therapies in oncology. The team is seeking a Clinical Trial Manager (CTM) who will serve as the study lead for ongoing and upcoming Phase 1/2 clinical programs.
This role is ideal for someone who thrives in a start-up environment, is comfortable being hands-on across multiple trial activities, and enjoys working in a highly collaborative setting where contributions are visible and impactful.
Key Responsibilities:
• Lead the planning, execution, and oversight of Phase 1/2 oncology clinical trials
• Manage timelines, study budgets, vendors, CROs, and site operations
• Oversee TMF quality, data review activities, safety review, and study documentation
• Partner cross-functionally with Clinical Development, Regulatory, Data Management, and Medical teams
• Ensure study delivery in accordance with GCP, ICH, SOPs, and regulatory requirements
• Represent Clinical Operations as the study lead in internal and external meetings
Requirements:
• 3 years of Clinical Trial Management experience, preferably in biotech
• Must have oncology trial experience (Phase 1/2 experience strongly preferred)
• Must have experience independently leading clinical studies
• Comfortable working in a lean, fast-paced start-up environment where adaptability is key
• Strong communication, organization, and vendor oversight skills
*Full benefits paid for the employee and their families!*
If you’re looking to make a meaningful impact and grow with a company at an exciting stage of development, we’d love to connect.
