Job Description
What You’ll Do:
Commercial & Strategic Contracting
- Draft, review, and negotiate commercial, vendor, professional services, technology, software, data, confidentiality, and strategic collaboration agreements.
- Advise on contract structure and risk allocation, including liability, indemnification, insurance, intellectual property, publications, data security, payment, and termination terms.
- Translate business objectives into clear contract terms, coordinate internal review and approvals, and move negotiations forward with counterparties.
- Support strategic partnerships, commercialization initiatives, health-system collaborations, and other business-critical programs with responsive, balanced legal guidance.
Clinical, Research, and Healthcare Agreements
- Draft and negotiate clinical trial and site agreements, amendments, material transfer agreements, research and collaboration agreements, business associate agreements, and data-sharing terms.
- Partner with Clinical, Corporate Development, Commercial, Finance, and other stakeholders to align scopes, budgets, payment terms, specimen use, publication rights, and intellectual property provisions.
- Identify and address healthcare, privacy, and compliance issues, including HIPAA and data-security requirements, and coordinate with subject-matter experts when specialized advice is needed.
- Prepare and maintain amendments and templates that accurately reflect entity changes, assignments, study updates, new workstreams, and agreed business terms.
- Drive agreements from initial issue spotting and redlines through clean copy, signature routing, confirmation of execution, and delivery of fully executed agreements.
Legal Operations & Cross-Functional Partnership
- Maintain accurate matter status in the contract lifecycle management system from intake through counterparty review, internal approval, signature, and closeout.
- Coordinate signature workflows, confirm required approvals and signature authority, and ensure executed agreements and related records are captured in the appropriate repository.
- Use and improve templates, fallback language, playbooks, and intake processes that help the business move efficiently while preserving appropriate legal controls.
- Provide clear status updates, surface dependencies and open issues early, and communicate legal recommendations in practical language to business partners and legal leadership.
Business Partnership and Risk Management
- Exercise sound judgment to distinguish material legal risks from acceptable business trade-offs, develop workable compromises, and escalate significant issues at the right time.
- Counsel stakeholders on confidentiality, publications, privacy, data security, insurance, and intellectual property and other recurring contracting risks.
- Collaborate with senior legal team members, internal subject-matter experts, and outside counsel on complex or specialized matters while retaining day-to-day ownership and follow-through.
Must Haves:
- A JD from an accredited law school and active membership in good standing with at least one state bar (California preferred, or eligible for Registered In-House Counsel status).
- 5+ years of relevant legal experience, with substantial responsibility for drafting and negotiating complex agreements; in-house experience in biotech, life sciences, diagnostics, medical device, or healthcare is strongly preferred.
- Demonstrated experience with a varied agreement portfolio, such as MSAs, SOWs, vendor and technology agreements, NDAs, clinical trial agreements, MTAs, research collaborations, and data-related agreements.
- Working knowledge of life sciences and healthcare contracting issues, including clinical research, HIPAA and data privacy, information security, publications, and intellectual property allocation.
- Hands-on experience using contract lifecycle management and electronic-signature systems to track matters, route approvals and signatures, and maintain reliable executed records.
- Excellent drafting, negotiation, project-management, and communication skills, with the ability to manage multiple matters and deliver clear, actionable advice.
- A practical, collaborative, and detail-oriented approach, strong ownership and urgency, and sound judgment that balances legal risk with clinical, commercial, and strategic goals.
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Freenome
View Company ProfileFreenome (operating under freenome.com) is a high-growth biotechnology and molecular diagnostics company that utilizes a proprietary AI-driven multiomics platform to pioneer non-invasive blood tests for early-stage cancer detection. Founded in 2014, the company shifts the paradigm of cancer screening away from isolated, single-analyte genomic testing. Instead, Freenome's platform integrates cell-free DNA (cfDNA), methylation patterns, genomic fragments, and programmatic protein biomarkers with advanced machine learning models to capture complex tumor signals and systemic immune responses at their earliest, most treatable stages. The company's foundational asset, the SimpleScreen colorectal cancer screening blood test, demonstrated exceptional clinical validation through its massive, prospective PREEMPT CRC clinical trial published in JAMA, meeting major efficacy endpoints for sensitivity and specificity. Capitalizing on this multiomic infrastructure, Freenome is aggressively scaling its diagnostic pipeline into a comprehensive Multi-Cancer Early Detection (MCED) portfolio targeting lung, pancreatic, and other high-mortality malignancies. Freenome has secured monumental, multi-million-dollar strategic commercialization and technology agreements with dominant industry pioneers, including a major global expansion partnership with Roche and an extensive distribution and licensing framework with Exact Sciences. Backed by over $1.4 billion in total funding from premier healthcare, tech, and life sciences institutional investors—including Andreessen Horowitz, Bain Capital Life Sciences, RA Capital, and Perceptive Advisors—Freenome entered into a definitive business combination agreement with Perceptive Capital Solutions Corp in late 2025 to transition into a publicly traded entity on the Nasdaq under the ticker FRNM. Headquartered in Brisbane, California, the organization operates sophisticated, CLIA-certified laboratory facilities and is led by industry veteran Dr. Aaron Elliott as Chief Executive Officer.
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