Clinical Trial Manager - Spain - Neuroscience / Ophthalmology / Infectious Disease

Medpace; Madrid; Híbrido; EUR 50.000 - 90.000; Jornada completa

Descripción de la vacante

Join a leading clinical research organization that is dedicated to making a difference in the world of health. This role offers the chance to manage clinical trials, ensuring compliance with regulations while leading a team to deliver high-quality results. With a focus on neuroscience and CNS, you will have the opportunity to work in your area of expertise or expand into new therapeutic areas. The organization provides a flexible work environment and a competitive compensation package, making it an ideal place for professionals passionate about advancing medical research. Be part of a team that positively impacts patients' lives globally.

Servicios

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Formación

• Minimum of 2 years of Clinical Trial Management experience required.
• 5+ years of Project Manager/Clinical Trial Manager experience at a CRO.

Responsabilidades

• Manage day-to-day operations of clinical projects according to regulations.
• Serve as primary Sponsor contact for operational project-specific issues.
• Develop operational project plans and manage site quality.

Conocimientos

Leadership Skills

Clinical Trial Management

Project Management

Risk Assessment

Educación

Bachelor’s degree in health or life science

Advanced degree in health or life science

Descripción del empleo

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Spain, particularly in our Madrid office. Clinical Trial Managers with expertise in Neuroscience and CNS are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. We provide remote flexibility only with relevant experience (after probation). We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.

Responsibilities

• 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.

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.
• 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.
• Strong leadership skills.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment.
• Competitive compensation and benefits package.
• Competitive PTO packages.
• Structured career paths with opportunities for professional growth.
• Company-sponsored employee appreciation events.
• Employee health and wellness initiatives.

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024.
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

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