Senior Clinical Project Manager

Advanced Resource Managers; Badajoz; Presencial; EUR 50.000 - 80.000; Jornada completa

Descripción de la vacante

A mid-sized CRO is seeking a Senior Project Manager to enhance their European team. This pivotal role involves managing clinical trials in Dermatology, serving as the primary liaison between internal teams and external stakeholders. The ideal candidate will have extensive experience in global clinical project management and be eager to contribute to large-scale Phase III trials.

Formación

• At least ten years of experience in the clinical research sector.
• Three years in a CRO.
• Experience in managing global Phase III trials.

Responsabilidades

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

Conocimientos

Project Management

Clinical Trials Management

Budget Management

Risk Management

Stakeholder Communication

Educación

Bachelor’s degree in a relevant field

Descripción del empleo

My client, a mid-sized CRO, is seeking a Senior Project Manager to strengthen their European team.

This role is pivotal for the successful management of clinical trials in Dermatology. The Senior Project Manager will serve as the primary liaison between internal teams and external stakeholders, ensuring all project objectives are met within the agreed timelines, budget, and quality standards.

We are looking for a candidate with at least seven years of global clinical project management experience, especially within European markets, and comprehensive knowledge of all phases of clinical trials from initiation to completion. The ideal candidate will be eager to contribute to a vibrant, expanding mid-sized CRO involved in large-scale multisite and global Phase III trials, and motivated to further their career.

Key responsibilities include:

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

Minimum requirements include:

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

If interested, please contact Vik Patel for further details.