CLC is the partner of choice for contracting strategy and services in support of the development of safe and effective products.

Jacquelyn E. Briggs, Esq.

Jacquelyn E. Briggs, Esq.

Life sciences attorney with extensive experience in contracting and clinical trials for drug development

Experienced Life Sciences Attorney

Jacquelyn is the Founder and CEO of Clinical Legal Consultants (CLC) with over 20 years of drug development experience across multiple therapeutic areas. With a B.S. in Biology and extensive work in preclinical research and clinical trials, she brings a uniquely integrated scientific and legal perspective to the industry. She also holds an M.S. in Regulatory Affairs for Drugs, Biologics, and Medical Devices, enhancing her ability to deliver strategic, multidisciplinary guidance. Since 2011, Jacquelyn has taught Pharmaceutical and Medical Device Law in Northeastern University’s Regulatory Affairs program and was recently appointed to the Food and Drug Law Institute’s 2026 Academic Advisory Committee.

Jacquelyn’s scientific, regulatory, and legal background enables her to add value across the research and development landscape. Her career began as a Clinical Research Coordinator and Pharmacy Technician in a Boston teaching hospital, followed by roles as a Clinical Research Associate overseeing Phase I - IV trials. After earning her J.D., she served as in-house counsel for both emerging R&D organizations and global commercial companies, focusing on complex contracting initiatives.

Her legal expertise, combined with broad experience in clinical research, and regulatory strategy allows her to bridge scientific, operational, and business considerations. This integrated approach strengthens legal integrity within organizations and supports efficient compliant product development.

AREAS OF EXPERTISE

  • Research Studies: Clinical Trial Agreements (CTAs) or other study agreements to support a range of research initiatives, including but not limited to Real-World Evidence Studies, Compassionate Use/Expanded Access Studies, or Investigator Initiated Studies, and all phases of clinical trials.
  • PHI/Privacy: Data Use Agreements, Business Associate Agreements, Data Processing Agreements and Standard Contractual Clauses.
  • Strategic Transactions: Collaborative Research Agreements, Sponsored Research Agreements, Material Transfer Agreements, and License Agreements.
  • Commercial Contracts: Master Services Agreements, Manufacturing Agreements, and Consulting Agreements.
  • Legal Operations: Template development; selection, implementation and oversight of Contract Lifecycle Management System (CLMS); continuous improvement of legal policies and procedures; training on various legal topics.

SERVICES

Effective Legal Solutions.

Clinical Operations Partnering

Drive the negotiations of CTAs and any other relevant ancillary agreements to ensure contracting is not the rate limiting step to site activation.

Contracts and Negotiations

Lead negotiations on a variety of agreements to deliver best outcomes for research, commercial and manufacturing initiatives.

Legal Operations

Support an organization with the development and management of legal tools, including the drafting of contract templates, managing the implementation and maintenance of a Contract Lifecycle Management System (CLMS), the continuous improvement of legal policies and procedures, and training on various legal topics.

Exceptional service that exceeded expectations.

Jacquelyn brings strong legal judgement and real-world life sciences contracting experience. She is an invaluable partner who can drive fast-moving projects with an impressive ability to navigate regulatory and scientific complexity.

Connacht Peterson

Biotech Executive

Doctor consulting with patient in medical office