Senior Clinical Project Manager

buscojobs España; Cáceres; Presencial; EUR 50.000 - 80.000; Jornada completa

Descripción de la vacante

A mid-sized Contract Research Organization is seeking a Senior Project Manager to enhance their European team. This pivotal role focuses on the execution of clinical trials in Dermatology, requiring extensive experience in project management and a strong understanding of global Phase III trials. The ideal candidate will lead communications with sponsors, oversee project planning, and ensure quality and risk management throughout the process.

Formación

• Minimum seven years of global clinical project management experience.
• Experience in global Phase III trials.
• At least three years in a CRO.

Responsabilidades

• Acting as the main contact for sponsors and leading client communications.
• Overseeing project planning and ensuring timely delivery of essential documents.
• Monitoring budgets and managing scope changes.

Conocimientos

Project Management

Clinical Trials

Communication

Risk Management

Educación

Bachelor’s degree in a relevant field

Descripción del empleo

My client, a mid-sized CRO, is looking for a Senior Project Manager to add value to their European team.

This role is crucial for the successful execution of clinical trials within Dermatology. The Senior Project Manager will serve as the primary liaison for internal teams and external stakeholders, ensuring all project tasks and deliverables are completed on time, within budget, and to quality standards.

We seek a candidate with a minimum of seven years of global clinical project management experience, particularly within European markets, and comprehensive knowledge of all stages of clinical trials from initiation to completion. The ideal candidate will be enthusiastic about contributing to a mid-sized Contract Research Organization involved in extensive multisite and global Phase III trials, and motivated to advance their career in a dynamic and growing company.

Key responsibilities include:

1. Acting as the main contact for sponsors and leading client communications.
2. Providing timely project updates.
3. Overseeing project planning, ensuring the delivery of essential documents and materials.
4. Maintaining audit readiness and managing quality and risk.
5. Monitoring budgets, managing scope changes, and leading trial execution.
6. Coordinating with team members and external vendors.

Requirements include:

• A Bachelor’s degree in a relevant field.
• At least ten years of experience in the clinical research sector.
• Minimum of three years in a CRO.
• Experience in global Phase III trials.