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Medpace

Global CRO delivering full-service clinical trials

Clinical Trial Manager - Neuroscience / Ophthalmology

Clinical Research OperationsConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • A bachelor's degree in a health or life science-related field is required.
  • Experience in Phases 1–4 is required; experience in Phases 2–3 is preferred.
  • At least 2 years of Clinical Trial Management experience is required; CRO experience is preferred.
  • At least 5 years of Project Manager or Clinical Trial Manager experience at a CRO is required for a remote-based role.
  • Experience managing overall project timelines is required.
  • Bid defense experience is preferred.
  • Strong leadership skills are required.

Responsibilities

  • Manage and provide accountability for day-to-day project operations as defined by the contract and in accordance with ICH/GCP and applicable laws, rules, and regulations.
  • Serve as the primary Sponsor contact for operational project-specific issues and study deliverables.
  • Maintain in-depth knowledge of the protocol, therapeutic area, and indication.
  • Provide cross-functional oversight of internal project team members and deliverables, including ensuring that necessary project-specific training is provided.
  • Review and provide input on the study protocol, edit check specifications, data analysis plan, and final study report, when applicable.
  • Develop operational project plans.
  • Manage risk assessment and execution.
  • Manage study vendors.
  • Manage site quality, including direct supervision of project Clinical Research Associates and oversight of monitoring deliverables.

Desired Qualifications

  • An advanced degree in a health or life science-related field.
  • Experience in Phases 2–3.
  • CRO experience.
  • Bid defense experience.

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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