Senior Clinical Project Manager

Advanced Resource Managers; Albacete; 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 oversee clinical trials in Dermatology. The role involves liaising with stakeholders, managing project timelines, and ensuring quality standards. Candidates should have extensive experience in clinical project management, particularly in global Phase III trials, and a passion for contributing to a growing company.

Formación

• Minimum of seven years of global clinical project management experience.
• Experience in global Phase III trials is essential.
• Three years in a CRO required.

Responsabilidades

• Act as the main contact for sponsors and lead client communications.
• Ensure the delivery of essential documents and materials.
• Monitor budgets, manage scope changes, and lead trial execution.

Conocimientos

Project Management

Clinical Trials

Stakeholder Communication

Budget 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 add value to their European team.

Role Overview

This role is a crucial hire 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.

Candidate Profile

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 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

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 materials.
4. Maintain audit readiness and manage quality and risk.
5. Monitor budgets, manage scope changes, and lead trial execution.
6. Coordinate with team members and external vendors.

Minimum Requirements

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

Application

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