Senior Clinical Project Manager

Advanced Resource Managers; Santander; 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 lead clinical trials in Dermatology. This role involves coordinating project tasks, managing budgets, and ensuring quality standards while serving as the primary liaison with sponsors. Ideal candidates will have extensive experience in clinical project management and a strong background in global Phase III trials.

Formación

• Minimum of seven years of global clinical project management experience.
• Experience in global Phase III trials and working in a CRO.
• Strong communication and leadership skills.

Responsabilidades

• Acting as the main contact for sponsors and leading client communications.
• Overseeing project planning and ensuring timely updates.
• Maintaining audit readiness and managing quality and risk.

Conocimientos

Project Management

Clinical Trials

Stakeholder Communication

Risk Management

Budget Monitoring

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 both internal teams and external stakeholders, ensuring that all project tasks and deliverables are achieved within the stipulated time frame, budget, and quality standards.

We seek a candidate who possesses a minimum of seven years of global clinical project management experience, particularly within European markets, and is well-versed in all stages of clinical trials from initiation to completion. The ideal individual will be enthusiastic about contributing to a mid-sized Contract Research Organization engaged in substantial multisite and global Phase III trials, and motivated to advance their career in a vibrant 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, 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.

A Bachelor’s degree in a relevant field and a minimum of ten years in the clinical research sector, including three years in a CRO, are required, along with experience in global Phase III trials.

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