Clinical Trial Manager (Oncology)

TL;DR

Clinical Trial Manager (Oncology): Leading the operational planning, conduct, and oversight of clinical studies with an accent on protocol adherence, regulatory compliance, and site management. Focus on driving recruitment strategies, ensuring data quality, and managing cross-functional study teams to deliver life-changing therapies.

Location: Must be based in Shanghai or Beijing, China

Company

hirify.global is a specialized CRO integrating clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences to improve the success rate of life-changing therapies.

What you will do

• Serve as the primary clinical point of contact for clients and internal study teams.
• Develop and manage study-related clinical documents, including plans, manuals, and training materials.
• Drive site feasibility, selection, and recruitment strategies to meet enrollment targets.
• Lead internal clinical team meetings and provide oversight for CRAs and CTAs.
• Ensure study conduct complies with protocol, SOPs, ICH-GCP, and regulatory requirements.
• Collaborate with data management and QA to ensure data quality and manage CAPA implementation.

Requirements

• Bachelor’s degree in a science or health-related field.
• 5-8 years of clinical research experience with significant clinical monitoring background.
• Must be based in Shanghai or Beijing.
• Proven experience in Oncology (Phase I) trials.
• Strong knowledge of ICH-GCP and regulatory requirements.
• Ability to manage clinical vendors and site budgets.

Nice to have

• Advanced degree in a science or health-related field.
• Experience with clinical trials in Taiwan.

Culture & Benefits

• Opportunity to work with a global leader in precision medicine and oncology.
• Focus on integrating advanced data sciences with clinical operations.
• Collaborative environment with a strong emphasis on scientific expertise.