Senior Clinical Project Manager

Advanced Resource Managers; Madrid; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

An established industry player is seeking a Senior Project Manager to enhance their European team. This pivotal role focuses on executing clinical trials in Dermatology, acting as the primary liaison between internal teams and external stakeholders. The ideal candidate will have extensive experience in global clinical project management, particularly within European markets, and a passion for contributing to a mid-sized Contract Research Organization involved in significant multisite Phase III trials. Join a vibrant and growing company where your expertise will drive success in clinical research.

Formación

• Minimum of seven years in global clinical project management.
• Experience in all stages of clinical trials from initiation to completion.

Responsabilidades

• Act as the main contact for sponsors and lead client communications.
• Ensure delivery of essential documents and maintain audit readiness.

Conocimientos

Clinical Project Management

Stakeholder Communication

Risk Management

Quality Assurance

Budget Management

Educación

Bachelor’s degree in a relevant field

Descripción del empleo

Direct message the job poster from Advanced Resource Managers

Head Of Life Science (International) at Advanced Resource Managers - EU / US

My client, who is a mid-sized CRO, is looking for a Senior Project Manager to add value to their European team.

This role serves as a crucial hire for the successful execution of clinical trials within Dermatology. Serving as the primary liaison for both internal teams and external stakeholders, these professionals ensure that all project tasks and deliverables are achieved within the stipulated time frame, budget, and quality standards.

We seek a candidate who possesses a minimum of seven years of global clinical project management experience, particularly within European markets, and is well-versed in 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 is motivated to advance their career in a vibrant and expanding company.

Key Responsibilities:

1. Acting as the main contact for sponsors
2. Leading client communications
3. Providing timely project updates
4. Ensuring the delivery of essential documents and materials
5. Maintaining audit readiness
6. Managing quality and risk
7. Managing scope changes
8. Leading trial execution while coordinating with team members and external vendors

Minimum Requirements:

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

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

Seniority level: Mid-Senior level

Employment type: Full-time

Job function: Research and Science

Industries: Staffing and Recruiting, Biotechnology Research, and Research Services