Senior Clinical Project Manager

buscojobs España; Ourense; 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 lead clinical trials in Dermatology. The role involves liaising with internal teams and external stakeholders, ensuring project tasks are completed on time and within budget. Candidates should have extensive experience in project management within the clinical research sector, especially in global Phase III trials.

Formación

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

Responsabilidades

• Act as the main contact for sponsors and lead client communications.
• Manage quality, risk, budgets, and scope changes.
• Lead trial execution and coordinate with team members and external vendors.

Conocimientos

Project Management

Communication

Quality Management

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 join their European team.

Role Overview

This position is crucial for the successful execution of clinical trials within Dermatology. The Senior Project Manager will serve as the primary liaison between internal teams and external stakeholders, ensuring all project tasks and deliverables are completed within the agreed time frame, budget, and quality standards.

Candidate Profile

We are seeking a candidate with a minimum of seven years of global clinical project management experience, especially within European markets. The candidate should be familiar with all stages of clinical trials from initiation to completion. An enthusiasm for working in a mid-sized Contract Research Organization involved in extensive multisite and global Phase III trials is essential, as is motivation to grow within a vibrant and expanding company.

Key Responsibilities

1. Act as the main contact for sponsors and lead client communications.
2. Provide timely project updates and oversee project planning.
3. Ensure the delivery of essential documents and maintain audit readiness.
4. Manage quality, risk, budgets, and scope changes.
5. Lead trial execution and coordinate with team members and external vendors.

Minimum Requirements

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

Application

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