
1001 - 5000 employees
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
💰 $75M Private Equity Round on 2015-12
Biotechnology • Healthcare Insurance • Pharmaceuticals
Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.
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1001 - 5000 employees
🧬 Biotechnology
⚕️ Healthcare Insurance
💊 Pharmaceuticals
💰 $75M Private Equity Round on 2015-12
Biotechnology • Healthcare Insurance • Pharmaceuticals
Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.
• Review, draft, and negotiate a variety of legal agreements including confidentiality agreements, clinical study agreements, and amendment agreements • Manage site agreements including the APAC region • Actively take part in setting up contracting strategies for assigned projects • Work closely with Clinical Operations study team to ensure deliverables are in alignment with defined study timelines
• Graduate, postgraduate, or 4-year college degree • Equivalent experience ideally in a legal or scientific or healthcare discipline • Relevant experience in drafting, reviewing and negotiating site Clinical Trial Agreements, vendor contracts and site Budget negotiations, but no less than 5 years’ experience • Experienced leading interactions with Study Teams and Sponsor • Strong relevant experience in drafting, reviewing and negotiating Clinical Trial Agreements and vendor contracts, as well as management, control and tracking of the contract process within APAC region • Strong site budget negotiation experience • Excellent organizational and communication skills and attention to detail.
• Health insurance • Mental wellness programs
Apply Now🔥 3 minutes ago
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