Senior Clinical Project Manager

buscojobs España; Badajoz; 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 critical role involves managing clinical trials in Dermatology, ensuring project tasks are completed on time, within budget, and to quality standards. The ideal candidate will have extensive experience in clinical project management and a passion for contributing to a growing organization.

Formación

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

Responsabilidades

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

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 within the agreed time frame, budget, and 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 will be enthusiastic about contributing to a mid-sized Contract Research Organization involved in substantial multisite and global Phase III trials, and motivated to grow their career in a vibrant and expanding company.

Key responsibilities include acting as the main contact for sponsors, leading client communications, providing timely project updates, overseeing project planning, ensuring the delivery of essential documents and materials, maintaining audit readiness, managing quality and risk, monitoring budgets, managing scope changes, and leading trial execution. The role also involves coordinating with team members and external vendors.

Requirements:

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