Senior Clinical Trial Manager – Oncology (Global)

Erasca, Inc.; United States; À distance; USD 145 000 - 190 000; Plein temps

Avantages offerts par ce poste

Annual bonus

Equity grant

401(k) plan

Comprehensive benefits

Paid time off

Résumé du poste

Erasca, Inc. is seeking a Clinical Trial Manager/Senior CTM to plan, implement, and manage global oncology trials from concept to close-out.

You will coordinate sites, vendors, budgets, and timelines, ensuring adherence to ICH-GCP and FDA/regulatory requirements while supporting cross-functional teams. The role emphasizes leadership in trial management, vendor oversight, and data integrity, with opportunities for career growth in a fast-paced, entrepreneurial environment.

Qualifications

• Preferred undergraduate degree in life sciences or related fields.
• For Clinical Trial Manager, 5+ years in oncology clinical operations; Senior CTM, 7+ years.
• Experience with trial setup, monitoring and close-out for US and non-US trials.
• Experience managing study vendors (CRO, laboratories, imaging).
• Excellent communication and project management skills.

Responsabilités

• Manage global Phase 1-3 oncology trials in compliance with ICH-GCP and regulatory requirements.
• Recruit study sites and cultivate investigator relationships.
• Participate in site and vendor selection, qualification and activation.
• Develop RFPs and assist in vendor contracting and negotiations.
• Oversee study vendors (CRO, IRT, labs, ECG/imaging) and material distribution.
• Monitor trial progress, enrollment, and study material inventory.
• Provide program updates to management and budget projections.

Connaissances

Trial management

Global collaboration

Regulatory knowledge

Communication

Self-starter

Formation

Life sciences degree

Pharmacy/Medicine/Nursing

Outils

EDC systems

IRT

Data management software

Description du poste

Erasca, Inc. is seeking a Clinical Trial Manager/Senior CTM to plan, implement, and manage global oncology trials from concept to close-out.

You will coordinate sites, vendors, budgets, and timelines, ensuring adherence to ICH-GCP and FDA/regulatory requirements while supporting cross-functional teams. The role emphasizes leadership in trial management, vendor oversight, and data integrity, with opportunities for career growth in a fast-paced, entrepreneurial environment.