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jobsVerified: 29 Sept 2026📍 Singapore

Site Contract Manager

P

Organising Institution / Firm

Precision Medicine Group

Quick Verified Facts

📅 Deadline

Rolling Basis (Official)

📍 Mode / Location

Singapore

💰 Stipend / Pay

Not Specified

🎓 Eligibility

Strong relevant experience (no less than 5 years) in drafting, reviewing, and negotiating Clinical Trial Agreements, vendor contracts, and site budget negotiations, particularly within the APAC region. Experience within the CRO, life science, biotech, or pharmaceutical industry is essential. Experience interacting with Global institutions with a focus on APAC ones. Graduate, postgraduate, or 4-year college degree, or equivalent experience, ideally in a legal, scientific, or healthcare discipline. Experienced in leading interactions with Study Teams and Sponsors. Preferred: Bachelor’s in law, scientific fields, or business administration. Fluency in English.

🛡️ Category

Job

Full Opportunity Brief

Site Contract Manager at Precision Medicine Group

Precision Medicine Group, a company focused on integrating clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences, is seeking an accomplished Site Contract Manager. This role involves reviewing, drafting, negotiating, and tracking various legal agreements, with a particular focus on clinical site agreements and vendor contracts within the APAC region.

Key Eligibility Criteria

  • Strong relevant experience (no less than 5 years) in drafting, reviewing, and negotiating Clinical Trial Agreements, vendor contracts, and site budget negotiations, particularly within the APAC region.
  • Essential experience within the CRO, life science, biotech, or pharmaceutical industry.
  • Experience interacting with Global institutions, with a focus on APAC ones.
  • Graduate, postgraduate, or 4-year college degree, or equivalent experience, ideally in a legal, scientific, or healthcare discipline.
  • Experienced in leading interactions with Study Teams and Sponsors.
  • Preferred: Bachelor’s in law, scientific fields, or business administration.
  • Fluency in English.

Responsibilities & Scope of Work

  • Review, draft, negotiate, and track a variety of legal agreements, including confidentiality agreements, master confidentiality agreements, clinical study agreements, and amendment agreements across various locations.
  • Actively participate in setting up contracting strategies for assigned projects.
  • Work closely with the Clinical Operations study team to ensure deliverables are in alignment with defined study timelines.
  • Fully responsible for Site Contract Management, from setting up site contracting strategy to execution of contracts.
  • Client-facing during the site contracting process.

Stipend, Compensation & Mode

Not Specified

Application Procedure & Required Documents

Interested candidates should apply directly through the official LinkedIn job posting. No specific documents beyond a standard resume/CV are mentioned in the provided content.

Official Notification & Contact Information

Verified by LexaUpdate Registry Desk
Access Official Application Portal↗
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