
1001 - 5000 employees
Founded 2000
☁️ SaaS
🤝 B2B
Legal • SaaS • B2B
Axiom is a company that provides legal services and law-related technology, simplifying the process of managing legal accounts for users. Their focus on accessibility and user-friendly processes highlights their commitment to modernizing the legal experience.
🔥 0 minutes ago
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1001 - 5000 employees
Founded 2000
☁️ SaaS
🤝 B2B
Legal • SaaS • B2B
Axiom is a company that provides legal services and law-related technology, simplifying the process of managing legal accounts for users. Their focus on accessibility and user-friendly processes highlights their commitment to modernizing the legal experience.
• Draft, review, negotiate, and manage a broad range of life sciences agreements, including: Clinical Trial Agreements (CTAs), Clinical Site Agreements (CSAs), Investigator Agreements, Confidentiality Agreements (NDAs/CDAs) • Support contract negotiations with clinical sites, hospitals, investigators, CROs, vendors, and strategic partners • Review and negotiate clinical trial budgets in collaboration with Clinical Operations, Finance, and external sites • Coordinate contract execution and maintain contract records using contract lifecycle management (CLM) systems or other contract repositories • Partner with Legal, Clinical Operations, Procurement, Regulatory Affairs, Finance, and Business Development teams to facilitate timely contract execution and study start-up activities • Track contract status, key milestones, amendments, renewals, and deliverables throughout the contract lifecycle
• 4+ years of experience supporting legal or contract management functions within the pharmaceutical, biotechnology, medical device, CRO, or life sciences industry • Experience drafting, reviewing, and negotiating Clinical Trial Agreements (CTAs) and Clinical Site Agreements (CSAs) required • Experience negotiating clinical trial budgets and vendor agreements strongly preferred • Familiarity with the clinical trial lifecycle and study start-up process • Knowledge of GCP, FDA regulations, and the clinical research environment is preferred • Experience working with CROs, sponsors, research institutions, or academic medical centres is highly desirable • Experience using contract lifecycle management (CLM) platforms or contract repositories preferred • Excellent organizational, communication, and stakeholder management skills
• health benefits • 401K • professional development tools and resources • learning and development programs
Apply Now🔥 16 hours ago
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