Clinical Project Manager

Jordan martorell s.l.; España; A distancia; EUR 40.000 - 70.000; A tiempo parcial

Descripción de la vacante

A dynamic opportunity for an experienced Freelance Clinical Project Manager to oversee clinical research projects across Spain. This role involves leading clinical trials, ensuring compliance, and managing stakeholders effectively. Applicants should possess a Bachelor’s degree in Life Sciences and have a minimum of 5 years' experience in clinical project management. The position offers competitive freelance rates and the chance to work on impactful projects in a collaborative environment.

Servicios

Competitive freelance rate

Opportunity to work on innovative clinical research

Collaborative and supportive project environment

Formación

• 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.

Responsabilidades

• Lead teams across all phases of clinical trials.
• Ensure compliance with regulatory requirements, timelines, and budgets.
• Manage study timelines, budgets, and resources.

Conocimientos

Project Management

Communication

Leadership

Organizational Skills

Educación

Bachelor’s degree in Life Sciences

Herramientas

Clinical Trial Management Systems

Descripción del empleo

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 [e-mail] with the subject line “Freelance Clinical Project Manager Application – [Your Name]”.