Full-Time

Senior Corporate Counsel

Ip, Technology, And Data

Posted on 11/15/2024

Clairo

Clairo

5,001-10,000 employees

Generates clinical evidence for trials

Biotechnology
Healthcare

Senior

Remote in USA

Fully remote; preference for candidates based in or near the Philadelphia metropolitan area.

Category
Legal
Intellectual Property (IP)
Legal & Compliance
Requirements
  • J.D. from an ABA-accredited law school.
  • Member in good standing of at least one state bar.
  • 6+ years of experience with a law firm and/or corporation working on technology-related legal issues globally; experience handling IP matters.
  • In-house experience at a multinational corporation in the pharmaceutical/biotech/CRO or Technology (software) industries and/or an understanding of clinical trials is preferred.
  • Familiarity with the fundamentals of IP law.
  • Experience drafting and negotiating contractual provisions and standalone agreements governing IP, AI, and data use.
  • Understanding of, and motivation to become an SME on, the key requirements of the EU AI Act.
Responsibilities
  • Providing advice and legal support to the Company in connection with intellectual property (“IP”), artificial intelligence (“AI”), data use and other technology-related issues.
  • Developing and implementing a cohesive global IP strategy, including as concerns the Company’s medical devices, software services, and AI tools.
  • Maintaining the Company’s existing IP portfolio (patents, trade secrets, trademarks).
  • Supporting the commercial contracts and procurement teams with the negotiation of IP, AI, and data use provisions in customer and vendor agreements and serving as the primary drafter and negotiator of complex standalone technology-related agreements (i.e., licensing, royalty, collaboration and data use agreements).
  • Enhancing the Company’s IP related policies, procedures, and training programs.
  • Participating in the drafting of policies and procedures relating to the use of AI.
  • Acting as a subject matter expert for internal stakeholders developing new products and updating existing product offerings by providing guidance as concerns data use best practices and the responsible use of AI.
  • Assisting with IP, AI and data use-related due diligence issues in connection with corporate transactions.
  • Collaborating with the data privacy, regulatory, IT Security, and quality assurance teams on data governance strategies and supporting the enhancement of the Company’s data retention policies and procedures.

Clario specializes in generating clinical evidence for medical research by combining scientific expertise with a wide range of endpoint technology. Their products support various types of clinical trials, including decentralized, hybrid, and site-based trials, allowing for flexibility in how studies are conducted. Clario stands out from competitors due to its extensive experience, having participated in nearly 19,000 clinical trials and achieved 870 regulatory approvals, which provides a high level of reliability in the data they produce. The company's goal is to empower partners in the healthcare industry to improve patient outcomes by providing comprehensive and trustworthy clinical evidence.

Company Stage

Growth Equity (Venture Capital)

Total Funding

$29.9M

Headquarters

London, United Kingdom

Founded

1972

Growth & Insights
Headcount

6 month growth

-6%

1 year growth

-6%

2 year growth

-6%
Simplify Jobs

Simplify's Take

What believers are saying

  • Clario's confidential IPO filing aiming for a $10 billion valuation indicates strong market confidence and potential for significant financial growth.
  • The acquisition of AI-powered software company ArtiQ enhances Clario's capabilities in respiratory solutions and AI, positioning it as a leader in clinical trial technology.
  • Achieving ISO 27001 certification demonstrates Clario's commitment to information security, which is crucial for maintaining client trust and regulatory compliance.

What critics are saying

  • The competitive landscape in clinical trial technology is intense, requiring continuous innovation to maintain a leading position.
  • Integration of new acquisitions like ArtiQ could pose challenges in terms of cultural and technological alignment.

What makes Clairo unique

  • Clario's nearly 50 years of experience and extensive portfolio of 19,000 clinical trials and 870 regulatory approvals set it apart in the clinical trial technology space.
  • The company's Trial Anywhere™ portfolio, which includes decentralized, hybrid, and site-based trials, offers unparalleled flexibility and scalability.
  • Clario's recent FDA 510(k) clearance for its SpiroSphere® with wireless ECG integration showcases its commitment to innovative, patient-friendly technology.

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Benefits

Competitive and equitable total rewards package

Physical, mental and financial health and wellness

Flexible working approach