Graduate Program : Frontend Engineer, 100% En remoto

Fortrea; España; Presencial; EUR 40.000 - 80.000; Jornada completa

Descripción de la vacante

An established industry player seeks a Senior Clinical Research Associate to drive excellence in neurology trials. In this pivotal role, you will ensure clinical studies meet the highest regulatory and quality standards while protecting patient safety. Your expertise in clinical monitoring and site management will be crucial as you coordinate projects and mentor new staff. With a commitment to advancing clinical research, this position offers a unique opportunity to make a significant impact on global health outcomes. Join a dynamic team where your contributions will shape the future of clinical trials and deliver life-changing treatments to patients worldwide.

Servicios

Competitive Compensation

Health and Wellness Programs

Flexible Work Arrangements

Professional Growth Opportunities

Formación

• 4+ years of clinical monitoring experience, especially in Neurology.
• Strong knowledge of regulatory and drug development processes.

Responsabilidades

• Conduct study site monitoring and maintain study files.
• Manage site-level project plans and ensure audit readiness.
• Mentor and assist with the development of new CRA staff.

Conocimientos

Clinical Monitoring

Regulatory Knowledge

Site Management

Communication Skills

Descripción del empleo

Join Fortrea as a SR Clinical Research Associate2 - Drive Clinical Excellence in Neurology Trials.

As a SRCRA, you will ensure clinical studies are conducted to the highest regulatory and quality standards, protecting patient safety and delivering reliable data. You’ll coordinate designated clinical projects as a Local Project Coordinator and may act as a local client contact as assigned. Your work will help shape the future of clinical research and provide life-changing treatments to patients worldwide.

Summary of Responsibilities:

• Conduct all aspects of study site monitoring (pre-study, initiation, routine, closeout visits) and maintain study files.
  
• Manage site-level implementation of project plans and ensure audit readiness.
  
• Ensure data integrity and patient protection by verifying adherence to protocols, informed consent, and regulatory requirements.
  
• Monitor, review, and resolve data discrepancies, and generate accurate trip reports.
  
• Act as Lead CRA or Local Project Coordinator, overseeing site activities and project progress.
  
• Serve as point of contact for clinical trial supplies and vendors.
  
• Mentor and assist with the development of new CRA staff as assigned.
  

Qualifications:

• 4+ years of clinical monitoring experience, mandatory experience in Neurology (preferably Ictus) therapeutic area.
  
• Strong knowledge of regulatory and drug development processes.
  
• Advanced site monitoring, site management, and registry administration skills.
  
• Fluent in local language and English, with excellent written and verbal communication.
  

Experience:

• 3+ years of experience in medical, clinical, pharmaceutical, or related fields.
  
• Local project coordination or project management experience.
  

Work Environment:

• 60-80% overnight travel, valid driver’s license required.
  

Benefits:
At Fortrea, we value our team members and offer a comprehensive benefits package, including competitive compensation, health and wellness programs, and opportunities for professional growth. You’ll also enjoy flexible work arrangements and the chance to make a meaningful impact in cutting-edge clinical research.

Your contribution to Fortrea’ s success:
In this role, you will help ensure the smooth execution of clinical trials and play a key role in delivering high-quality data and compliance. Your efforts will contribute directly to Fortrea’ s mission of advancing clinical research and improving global health outcomes. Ready to make an impact? Join us!

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