Corporate Counsel

Job Locations US-NJ-Florham Park
ID
2022-1916
Category
Legal
Type
Regular Full-Time

Overview

At Celularity, we are passionate about our mission to lead the next evolution of cellular medicine by developing off-the-shelf placental derived allogeneic cell therapies targeting hard-to-treat and unmet needs of cancer, infectious and degenerative diseases. We use a pioneering technology platform with groundbreaking basic and translational research to advance the development of cellular medicines that overcome barriers of scale, quality, and economics.

 

Responsibilities

  • Serve as a business and legal partner for the Clinical organization.
  • Provide timely, pragmatic and accurate counsel to clients on a variety of legal, regulatory and compliance topics.
  • Draft and negotiate agreements, including clinical trial agreements, CRO agreements, vendor agreements, confidentiality agreements and MSAs.
  • Support all aspects of clinical trial startup and continuation, both in the U.S. and potentially ex-U.S.
  • Work collaboratively with clinical colleagues to develop pragmatic, creative and compliant solutions.
  • Evaluate risks regarding business decisions and clinical operations, apply effective risk management techniques and offer proactive advice on potential legal issues.
  • Effectively communicate and negotiate with external parties (e.g., clinical trial sites, academic institutions, government agencies, etc.).
  • Demonstrate strong communication skills (both written and verbal) and the ability to drive discussions to effective and actionable conclusions.
  • Other duties and projects, as needed.

Qualifications

  • J.D. degree from a U.S. accredited law school.
  • 6+ years of legal experience.
  • Prior professional experience in-house at a life science/pharmaceutical company or healthcare institution, working on healthcare and clinical trial-related matters, preferred but not required.
  • Experience drafting and negotiating agreements, including clinical trial site agreements, CRO agreements, vendor agreements, confidentiality agreements and MSAs.
  • Knowledge of current laws, regulations and industry standards governing clinical trials, such as FDA regulations, ICH Guidelines and GCPs.

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