Skip navigation


Established in 1992, Medpace has partnered with leading pharmaceutical and biotech companies to bring promising new drugs to market. Medpace combines efficient clinical trial management with comprehensive regulatory consulting to provide Sponsors with exceptional support during the drug development process.

The integrated services at Medpace include: clinical development plan preparation, project management, regulatory document preparation, safety surveillance, clinical monitoring, data management, statistical analysis, medical writing, quality assurance auditing, and US and international regulatory submissions.

At Medpace, proven leaders in medical and scientific research monitor every project. The therapeutic focus and experience of the Medpace team, which includes on-staff physicians, reduces the need for client oversight, review, and training. In addition, Medpace physicians have first-hand experience working with regulatory agencies to successfully guide projects through the complexities of the regulatory process. The medical expertise and regulatory guidance provided by Medpace leads to reduced costs and increased efficiencies for our valued customers.

Medpace brings together an exceptionally well-qualified team of medical and scientific personnel for every project. This team-based approach, combined with comprehensive training programs, active career development and cross-training opportunities, has significantly reduced attrition. This provides Sponsors with personalized service and the potential for long-term partnerships.

Medpace offers a variety of leading edge technologies to track, interpret, and communicate information in the most timely, secure, and cost-effective manner. ClinTrak®, a web-based, proprietary research management system designed by Medpace, offers access to near real-time study data and metrics. 


Medpace offers an array of benefits. We have an employee-focused environment with professional training and career development opportunities. We strive for success in all aspects of our business, including satisfied employees.
  • Medical Care and Dental Care
  • Short-Term & Long-Term Disability
  • Life & AD&D Insurance
  • Medical and Dependent care reimbursement accounts
  • Paid Vacation Days - 15 per year, 20 days per year after 5 years of service
  • Paid Sick Days
  • Average of 10 paid holidays per year
  • Business Casual Work Environment - The dress code Monday through Thursday is business casual and associates may wear casual attire on Fridays


Medpace's mission is to improve worldwide health care through the highest quality and cost-effective clinical research, while providing a safe, ethical, and satisfying work environment to its associates.


Medpace employees are our most valuable asset. We focus on providing open communication and take an interest in all employee ideas and concerns. We invite you to apply to join our exciting, high-quality, people-oriented, unique medical research organization.


Medpace is a science-based company bringing extensive experience in clinical research to the drug development process. The medical expertise within Medpace allows for a reduced level of sponsor oversight, review, and training. At Medpace, we specialize in managing studies in the cardiovascular and metabolic fields, which enable our clients to look to us for more than just temporary staffing. Our focused approach gives us an intimate familiarity with the clinical trial issues in these fields, bringing expertise and understanding to all aspects of the drug development process. We are looking for qualified candidates who are willing to be part of a team and committed to providing a high-quality product.

Code of Ethics

General Code of Ethics

All Medpace associates are held to the highest standards of ethical behavior in all business dealings and must fully comply with all applicable laws. Honesty, confidentiality, integrity, and adherence to Standard Operating Procedures and Good Clinical Practice Guidelines are our governing principles. Given the nature of our business, anything less could compromise public safety. Associates are responsible for understanding and complying with all company policies and Standard Operating Procedures that define the manner in which all business related activities are to be conducted. All associates are held accountable for their actions and are required to report unethical or unlawful activities.

Associates who are Managers and Executive Officers are also responsible for ensuring that the associates they supervise are knowledgeable and in compliance with all company policies related to their job responsibilities. Managers and Executive Officers are expected to maintain and promote open communication throughout the organization and continuously strive to implement best industry practices.

Furthermore, Medpace maintains a Policies Manual which must be read, understood, and acknowledged (by signature) by all associates. Company policies, including but not limited to confidentiality, harassment, conflicts of interest, whistle blower, and standards of conduct are clearly documented in the manual. Associates who do not comply with policies defined in the manual are subject to disciplinary action.


Employee: This term is used to describe individuals who work for Medpace for wages. Employees receive paychecks from Medpace while working or are on a form of company approved leave. This term is used in policies and standard operating procedures.

Associate: This term is used to describe all employees of Medpace as well as other individuals working at a Medpace work site. This might include independent contractors and freelance workers. All associates are expected to abide by applicable policies and standard operating procedures.

Financial Code of Ethics

Medpace upholds the following Financial Code of Ethics, which is applicable to its employees, directors, and officers. Furthermore, the Chief Executive Officer (CEO), the Chief Financial Officer (CFO) and others who perform equivalent responsibilities, or play a significant role in financial reporting, attest on an annual basis that they have read, understand and adhere to the principles defined in the code as follows:

  • Financial information is reported completely, honestly, accurately and in a timely manner.

  • The CFO is responsible for ensuring that he/she and all financial officers operate within the law and other applicable rules and regulations, and at the highest level of integrity when handling all aspects of financial reporting.

  • The CFO, CEO, and members of the Executive Committee are responsible for promoting honest and ethical conduct, including recognizing actual or potential conflicts of interest amongst themselves and others, and for taking appropriate action to prevent collusion and inappropriate or unlawful financial transactions.

  • Suspected or actual financial wrongdoing is promptly reported to the chairman of the Audit Committee or the Corporate Compliance Officer (see Policies Manual).

  • Confidential information is safeguarded except when authorized or required to disclose such information.

  • Any associate who violates this code of ethics is subject to disciplinary action, which may include termination of employment and or legal action.

  • The board of directors is responsible for considering any request for a waiver of, or amendment to, this financial code. Any waiver or amendment must be supported by a supermajority vote (at least 66%) of the directors in order for it to be approved. Furthermore, all directors must be polled vs. polling a quorum of less than the complete board. All waivers or amendments are disclosed timely as provided by law.

EO/AA Employer M/F/Disability/Vets