Senior Clinical Project Manager

Advanced Resource Managers; Castellón de la Plana; Presencial; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A mid-sized Contract Research Organization is seeking a Senior Project Manager to oversee clinical trials in Dermatology. The role involves managing project tasks, liaising with stakeholders, and ensuring quality standards are met. The ideal candidate has extensive project management experience and is eager to grow within a dynamic company.

Formación

• Minimum seven years of global clinical project management experience.
• Experience in global Phase III trials.

Responsabilidades

• Acting as the main contact for sponsors and leading client communications.
• Overseeing project planning and ensuring the delivery of essential documents.

Conocimientos

Project Management

Communication

Educación

Bachelor’s degree

Descripción del empleo

My client, a mid-sized CRO, is looking for a Senior Project Manager to join 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 meet quality standards.

We seek a candidate with a minimum of seven years of global clinical project management experience, especially within European markets, and comprehensive knowledge of all stages of clinical trials from initiation to completion. The ideal candidate is enthusiastic about contributing to a mid-sized Contract Research Organization involved in large multisite and global Phase III trials and is motivated to grow their career in a dynamic and expanding 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 and 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 in the clinical research sector, including three years in a CRO.
• Experience in global Phase III trials.

If you are interested in this role, please contact Vik Patel.