Senior Clinical Project Manager

Advanced Resource Managers; Las Palmas de Gran Canaria; Presencial; EUR 70.000 - 90.000; 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 projects are completed on time and within budget. Ideal candidates will have extensive experience in clinical project management and a passion for advancing their careers in a dynamic environment.

Formación

• Minimum of seven years of global clinical project management experience.
• Minimum of ten years in the clinical research sector, including three years in a CRO.

Responsabilidades

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

Conocimientos

Project Management

Clinical Trials

Educación

Bachelor’s degree

Descripción del empleo

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

This role is vital for the successful execution of clinical trials within Dermatology. The Senior Project Manager will act as the primary liaison for internal teams and external stakeholders, ensuring all project tasks and deliverables are completed on time, within budget, and meet quality standards.

Requirements:

1. Minimum of seven years of global clinical project management experience, especially within European markets.
2. Well-versed in all stages of clinical trials from initiation to completion.
3. Enthusiastic about working in a mid-sized Contract Research Organization involved in multisite and global Phase III trials.
4. Motivated to advance their career in a vibrant and expanding company.

Key Responsibilities:

• Act as the main contact for sponsors and lead client communications.
• Provide timely project updates.
• Oversee project planning, ensuring the delivery of essential documents and materials.
• Maintain audit readiness and manage quality and risk.
• Monitor budgets, manage scope changes, and lead trial execution.
• Coordinate with team members and external vendors.

Qualifications:

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

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