Clinical Project Manager

buscojobs España; Cádiz; A distancia; EUR 50.000 - 80.000; Jornada completa

Descripción de la vacante

A growing biotech company is seeking a Clinical Project Manager to lead international clinical trials from a remote location. Responsibility includes managing trial operations, ensuring compliance, and collaborating with cross-functional teams in a dynamic environment. Join a mission-driven team that values innovation and flexibility.

Servicios

Flexible remote-first working setup

Competitive compensation and benefits

Work with an innovative biotech company

Formación

• Solid experience in clinical project management, especially in global trials.
• Excellent understanding of regulatory guidelines (ICH-GCP).
• Comfortable working remotely in a dynamic environment.

Responsabilidades

• Manage the full lifecycle of global clinical trials from planning to close-out.
• Lead cross-functional teams and oversee vendor relationships.
• Ensure compliance with regulations and monitor project timelines.

Conocimientos

Leadership

Communication

Organizational

Regulatory Guidelines Understanding

Descripción del empleo

Clinical Project Manager (Global Clinical Trials)

Location: Remote based in Spain or anywhere in the European Union

Employment Type: Full-time

We are currently recruiting on behalf of our client, an exciting and growing biotech company focused on bringing innovative therapies to market. As part of their expansion, they are seeking a Clinical Project Manager to join their global team and lead international clinical trials across multiple regions.

About the Role :

In this role, you will oversee global clinical study operations from start-up through close-out. The ideal candidate will have proven experience managing international clinical trials and thrive in a fast-paced, agile biotech environment. You will collaborate with cross-functional teams, CROs, and vendors to ensure successful study execution aligned with timelines, quality standards, and regulatory requirements.

Key Responsibilities :

1. Manage the full lifecycle of global clinical trials, including planning, execution, and close-out.
2. Lead and coordinate cross-functional teams, both internally and externally.
3. Oversee third-party vendors and CRO relationships to ensure study deliverables.
4. Ensure compliance with ICH-GCP, SOPs, and all applicable regulations.
5. Develop and review study protocols and operational documents.
6. Monitor project timelines, budgets, and risks, implementing mitigation plans as needed.
7. Serve as the primary contact for internal stakeholders and external partners.

Candidate Profile :

• Solid experience in clinical project management, especially in global trials.
• Excellent understanding of clinical development and regulatory guidelines (ICH-GCP).
• Strong communication, leadership, and organizational skills.
• Comfortable working remotely in a dynamic, matrixed environment.
• Must be EU-based and eligible to work within the EU.

Desirable (Nice to Have) :

• Experience in neuroscience or ophthalmology.
• Exposure to both early and late-phase trials.

Why Join?

• Work with a biotech company that values innovation, transparency, and collaboration.
• Be part of a passionate, mission-driven team.
• Flexible remote-first working setup.
• Competitive compensation and benefits.

If you're ready to advance your clinical career with a company where you can make a real impact, we’d love to hear from you.