Site Contract Manager

🔥 0 minutes ago

🌐 Singapore, Taiwan – Remote

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⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 20%

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Logo of Precision Medicine Group

Precision Medicine Group

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Review, draft, negotiate, and track confidentiality agreements, master confidentiality agreements, clinical study agreements, and amendment agreements across various locations • Set up contracting strategies for assigned projects • Manage site contracting from setting up site contracting strategy through contract execution • Work closely with Clinical Operations study teams • Ensure deliverables align with defined study timelines • Act as a client-facing representative during the site contracting process • Lead interactions with Study Teams and Sponsors • Develop, maintain, and strengthen relationships with internal and external stakeholders • Handle sensitive issues with discretion • Execute time-sensitive matters while maintaining accuracy and attention to detail

🎯 Requirements

• Strong relevant experience drafting, reviewing, and negotiating Clinical Trial Agreements and vendor contracts • Experience managing, controlling, and tracking contract processes within the APAC region • Strong site budget negotiation experience • Experience within a CRO, life science, biotech, or pharmaceutical industry is essential • Experience interacting with global institutions, with a focus on APAC institutions • Excellent organizational and communication skills and attention to detail • Graduate, postgraduate, or 4-year college degree • Equivalent experience ideally in a legal, scientific, or healthcare discipline • At least 5 years of experience drafting, reviewing, and negotiating site Clinical Trial Agreements, vendor contracts, and site budget negotiations • Experience leading interactions with Study Teams and Sponsors • Proficiency in setting up contracting plans and guides for CTA and budget negotiations • Proficiency handling relationships with study teams, sites, and sponsors • Proficiency in MS Office software programs and computer applications • Ability to work independently and cooperatively in a virtual environment • Some domestic and occasional international travel including overnight stays

🏖️ Benefits

• Regular full-time employment • Remote work arrangement in Singapore or Taiwan • Some domestic and occasional international travel including overnight stays

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