Site Contract Manager (Clinical Trials)

Location: Remote from Singapore or Taiwan; some domestic and occasional international travel, including overnight stays, is required.

Company

hirify.global is a contract research organization integrating clinical trial execution with scientific expertise, laboratory capabilities, and advanced data sciences for life sciences clients.

What you will do

• Review, draft, negotiate, execute, and track confidentiality agreements, Clinical Trial Agreements, vendor contracts, and amendments.
• Develop contracting strategies and plans for assigned clinical study projects across the APAC region.
• Lead site contract management from strategy setup through execution, including site budget negotiations.
• Coordinate closely with Clinical Operations study teams and ensure contracting deliverables meet study timelines.
• Manage client-facing interactions with study sites, sponsors, global institutions, and internal stakeholders.
• Handle multiple time-sensitive agreements independently while maintaining accuracy, discretion, and strong relationships.

Requirements

• At least 5 years of relevant experience drafting, reviewing, and negotiating site Clinical Trial Agreements, vendor contracts, and site budgets.
• Experience managing clinical site agreements and contract processes across APAC, including interactions with global institutions.
• Experience in a CRO, life sciences, biotech, or pharmaceutical organization.
• Graduate, postgraduate, or four-year college degree; legal, scientific, healthcare, or equivalent experience is suitable.
• Experience leading interactions with study teams and sponsors, with strong organizational, written communication, and negotiation skills.
• Fluent English required; proficiency in Microsoft Office and computer applications.

Nice to have

• Bachelor’s degree in law, a scientific field, or business administration.
• Experience creating contracting plans and guides for Clinical Trial Agreement and budget negotiations.
• Experience managing relationships with study teams, sites, and sponsors.

Culture & Benefits

• Remote work arrangement from Singapore or Taiwan within a virtual environment.
• Independent work combined with collaboration across study teams and global stakeholders.
• Fast-paced environment involving time-sensitive clinical contracting deliverables.
• Opportunity to contribute to clinical studies supporting life-changing therapies.
• Occasional domestic and international travel is part of the role.