Senior Clinical Project Manager

buscojobs España; Málaga; 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 enhance their European team. This role focuses on managing clinical trials in Dermatology, ensuring project deliverables meet time, budget, and quality standards. The ideal candidate will have extensive experience in clinical project management and a passion for advancing their career in a dynamic environment.

Formación

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

Responsabilidades

• Acting as the main contact for sponsors.
• Leading client communications.
• Overseeing project planning.

Conocimientos

Project Management

Clinical Trials

Communication

Educación

Bachelor’s degree

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 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 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
2. Leading client communications
3. Providing timely project updates
4. Overseeing project planning
5. Ensuring the delivery of essential documents and materials
6. Maintaining audit readiness
7. Managing quality and risk
8. Monitoring budgets
9. Managing scope changes
10. Leading trial execution
11. Coordinating with team members and external vendors

Requirements include a Bachelor’s degree in a relevant field and at least ten years of experience in the clinical research sector, including three years in a CRO, with experience in global Phase III trials.

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