Clinical Trial Manager – Immunology/ID (Madrid) Remote

Jobbydoo; Madrid; On-site; EUR 70,000 - 90,000; Full time

Benefits offered by this job

Equity grants

On-site with occasional WFH

Job summary

Medpace is seeking a Clinical Trial Manager for Madrid to support operations on ICH/GCP-compliant trials in Immunology and Infectious Diseases. The role focuses on overseeing day‑to‑day project activities, serving as sponsor contact, and ensuring study deliverables align with protocol and timelines.

The successful candidate will manage cross‑functional teams, supervise CRAs, and drive risk mitigation while maintaining strong knowledge of the therapeutic area.

Qualifications

• Bachelor’s degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred.
• Experience in Phases 1-4; Phases 2-3 preferred.
• Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred.
• Management of overall project timeline.
• Bid defense experience preferred.
• Strong leadership skills.

Responsibilities

• Manage day-to-day operations of the project per contract and ICH/GCP.
• Serve as primary Sponsor contact for operational issues and study deliverables.
• Maintain knowledge of protocol, therapeutic area, and indication.
• Provide cross-functional oversight of internal project team and training.
• Review study protocol, edit check specs, 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 and supervision of project CRAs.

Skills

CTR management

Leadership

Timeline management

Bid defense

Phases 1-4 experience

Education

Bachelor’s degree in health or life sciences

Advanced degree preferred

Job description

Medpace is seeking a Clinical Trial Manager for Madrid to support operations on ICH/GCP-compliant trials in Immunology and Infectious Diseases. The role focuses on overseeing day‑to‑day project activities, serving as sponsor contact, and ensuring study deliverables align with protocol and timelines.

The successful candidate will manage cross‑functional teams, supervise CRAs, and drive risk mitigation while maintaining strong knowledge of the therapeutic area.