Remote Clinical Trial Manager — Neuroscience & Ophthalmology

Medpace; Greater London, Stirling; Híbrido; GBP 65.000 - 90.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible work environment

Competitive compensation and benefits

Competitive PTO packages

Structured career paths with growth

Company-sponsored employee events

Employee health and wellness

Descripción de la vacante

Medpace, the leading CRO, is hiring Clinical Trial Managers in the United Kingdom, with roles in London and Stirling. The positions welcome Neuroscience/CNS expertise and allow remote flexibility after probation, depending on experience and performance.

A competitive salary/bonus program and equity grants are offered to successful candidates. These roles require 2+ years of CTM experience and a strong background in ICH/GCP compliance, with a track record across Phases 1-4 and CRO work.

Formación

• Bachelor's degree in health or life or life sciences required; advanced degree preferred.
• Experience in Phases 1-4; Phases 2-3 preferred.
• Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred.
• 5+ years of Project Manager/Clinical Trial Manager experience at a CRO required for a remote-based role.
• Management of overall project timeline.
• Bid defense experience preferred; and
• Strong leadership skills.

Responsabilidades

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

Conocimientos

Phases 1-4 experience

Clinical Trial Manager experience

CRO experience preferred

Project timeline management

Leadership skills

Bid defense experience

Experience as CTM/PM in CRO

Educación

Bachelor's degree in health or life sciences

Advanced degree in health or life sciences preferred

Descripción del empleo

Medpace, the leading CRO, is hiring Clinical Trial Managers in the United Kingdom, with roles in London and Stirling. The positions welcome Neuroscience/CNS expertise and allow remote flexibility after probation, depending on experience and performance.

A competitive salary/bonus program and equity grants are offered to successful candidates. These roles require 2+ years of CTM experience and a strong background in ICH/GCP compliance, with a track record across Phases 1-4 and CRO work.