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Medpace

Global CRO delivering full-service clinical trials

Corporate Counsel 1

Legal Counsel & Legal SupportConfirmed live in the last 24 hours
Full-timeCincinnati, OH, USANo salary listed

About the Job

Requirements

  • Juris Doctorate degree from an accredited law school.
  • Licensed in Ohio or eligible to become licensed.
  • Three to five years of relevant experience at a law firm or in-house, or a combination of both.
  • Knowledge of contracts, corporate law, compliance, governance, collections, and general litigation.
  • Negotiation, drafting, analytical, and interpersonal skills.
  • Ability to explain complex legal concepts in clear, business-friendly terms.
  • Ability to take initiative and interact cross-functionally as part of a team.
  • Ability to manage multiple priorities and meet deadlines.

Responsibilities

  • Review, draft, and negotiate domestic and foreign agreements, including commercial and vendor agreements and software-as-a-service and technology licenses.
  • Manage third-party contracting processes and workflows.
  • Assist the legal team in drafting and updating corporate compliance policies and standard operating procedures.
  • Serve as a point of contact for global privacy and data protection matters.
  • Advise management on corporate policies, bylaws, and resolutions.
  • Monitor changes in local, state, federal, and foreign laws and regulations, including government contracting, and advise management accordingly.
  • Identify potential legal and business risks in operations, strategic planning, and business development activities.
  • Escalate legal risks to members of management with recommendations for resolution.
  • Identify appropriate outside counsel and oversee or coordinate outsourced legal work.
  • Provide or arrange legal services for enterprise-wide or entity-wide support and administrative functions.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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