Clinical Project Manager

JR Spain; Madrid; Híbrido; EUR 50.000 - 85.000; A tiempo parcial

Descripción de la vacante

A clinical research organization is seeking a Freelance Clinical Project Manager to lead and drive clinical research projects in Spain. This role requires overseeing all phases of clinical trials, ensuring compliance with regulatory standards, and managing timelines and budgets. The ideal candidate should have at least 5 years of clinical project management experience and strong leadership skills. Competitive freelance rates and opportunities to work on innovative clinical research are offered, along with a collaborative project environment.

Servicios

Competitive freelance rate

Opportunity to work on innovative research

Supportive project environment

Formación

• Minimum 5 years of experience in clinical project management.
• Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
• Proven ability to manage global clinical trials.

Responsabilidades

• Plan, initiate, and manage Phase I–IV clinical trials across multiple therapeutic areas.
• Ensure clinical studies are conducted in compliance with ICH-GCP, regulatory guidelines, and company SOPs.
• Prepare and present study updates to senior leadership and sponsors.

Conocimientos

Leadership

Communication

Organizational skills

Educación

Bachelor's degree in Life Sciences or related field

Herramientas

Clinical trial management systems

Descripción del empleo

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Freelance Clinical Project Manager Opportunity

Position: Freelance Clinical Project Manager

Location:- All Spain- Hybrid (occasional travel when required)

Contract Type: Freelance / Contract

Duration: 6-12 months

Rate: Competitive / DOE (Depending on Experience)

Are you an experienced Clinical Project Manager looking for your next freelance opportunity? We are seeking a highly motivated Freelance Clinical Project Manager to oversee and drive our clinical research projects to successful completion.

About the Role:

As a Clinical Project Manager, you will lead teams across all phases of clinical trials, ensuring compliance with regulatory requirements, timelines, and budgets. You will be the main point of contact between sponsors, CROs, vendors, and internal stakeholders.

Key Responsibilities:

• Plan, initiate, and manage Phase I–IV clinical trials across multiple therapeutic areas
• Ensure clinical studies are conducted in compliance with ICH-GCP, regulatory guidelines, and company SOPs
• Manage study timelines, budgets, and resources
• Oversee site selection, initiation, monitoring, and close-out activities
• Coordinate with vendors, CROs, and internal stakeholders
• Mitigate risks and resolve issues to keep trials on track
• Prepare and present study updates to senior leadership and sponsors

Requirements:

• Bachelor’s degree in Life Sciences or related field (advanced degree a plus)
• Minimum 5 years of experience in clinical project management
• Strong knowledge of GCP, ICH guidelines, and regulatory requirements
• Proven ability to manage global clinical trials
• Excellent communication, leadership, and organizational skills
• Ability to work independently in a remote environment
• Proficiency in clinical trial management systems and tools

What We Offer:

• Competitive freelance rate
• Opportunity to work on innovative and meaningful clinical research
• Collaborative and supportive project environment

Ready to Apply?

Please send your CV, availability, and rate expectations to [emailprotected] with the subject line “Freelance Clinical Project Manager Application – [Your Name]”.