Senior Clinical Trial Manager, APAC, Clinical Operations (Based in China)

The role

You will plan, execute, and manage clinical trials across multiple global sites. You will collaborate with cross-functional teams and external vendors to ensure successful implementation in accordance with regulatory requirements.

What you will do

• Develop and execute global site management plans including timelines, budgets, and resource allocation
• Oversee site selection, initiation, and monitoring activities
• Coordinate with vendors including CROs, central laboratories, and other service providers
• Manage trial-related documents including protocols, investigator brochures, and informed consent forms
• Implement risk mitigation strategies and address issues and deviations
• Serve as the primary point of contact for investigative sites
• May function as subject matter expert for clinical systems such as eTMF or CTMS
• Contribute to the development and implementation of process improvements and best practices
• Keep abreast of industry trends, regulatory guidelines, and emerging technologies

Required qualifications

• B.S./B.A. in life science or related field
• 6+ years of experience in clinical trial management within the pharmaceutical, biotechnology, or CRO industry
• Phase 1-3 Oncology experience required
• Phase 1-3 global trial management experience required
• Direct experience overseeing global CROs and other study vendors
• Experience with APAC region, including China (required)
• Solid attention to detail and excellent organizational skills
• Strong interpersonal and communication skills (both written and oral)
• Ability to establish priorities, excellent sense of urgency and a strong desire to collaborate
• Creative problem-solving skills
• Self-motivated and adaptable in a dynamic, nimble, start-up environment
• Strong computer skills and experience using Microsoft Office applications, CTMS, eTMF, IRT and EDC platforms

Nice to have

• Experience with Taiwan, Hong Kong, Japan and South Korea
• 3+ years on-site monitoring experience

Benefits

• Annual target bonus
• Equity
• Comprehensive suite of competitive benefits

Before you apply

• This role requires the individual to be based in China
• Relocation to China will not be offered

About the company

Parabilis Medicines is a clinical-stage biopharmaceutical company dedicated to creating medicines for patients with serious diseases by unlocking biologically important targets. The company has pioneered a new class of alpha-helical peptides called Helicons.