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Clinical Research Associate Job at Fortrea, Warsaw | Life Sciences Candidates, Apply Now

Clinical Research Associate Job at Fortrea, Warsaw | Life Sciences | Apply Now

The future of clinical innovation isn’t just about laboratory breakthroughs; it’s about the dedicated professionals who ensure those breakthroughs are safe, ethical, and meticulously documented. If you are an experienced monitor ready to step into a role that offers deep study knowledge and long-term project ownership, the Clinical Research Associate Job at Fortrea in Warsaw is your next career milestone. By working exclusively with a single sponsor, you move beyond being a generalist and become a strategic partner in the development of life-changing therapies.

 

About the Company

Fortrea is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. The organization provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development and technology solutions across more than 20 therapeutic areas. A Fortrea career is defined by the “Fortrea FOUR” culture: Forward Together, Own It, Uphold Integrity, and Respect People. This commitment ensures that every employee is empowered to find solutions and deliver results while keeping patient safety at the heart of their work. Operating in over 90 countries, Fortrea offers a flexible and scalable Functional Service Provider (FSP) model that allows specialists to embed themselves within a sponsor’s team. This model is ideal for those seeking a Life Sciences Job that offers the stability of a major CRO with the focused environment of a pharmaceutical sponsor.

Key Responsibilities

In this Clinical Research Associate Job, the specialist acts as the primary liaison between the clinical study site and the sponsor. The role is focused on interventional studies, requiring a high degree of precision in site management and data integrity.

  • Site Lifecycle Management: Perform comprehensive site monitoring activities, including site selection, initiation, routine monitoring, and close-out visits to ensure adherence to study protocols.

  • Safety & Data Quality: Review Case Report Forms (CRFs) and perform Source Data Verification (SDV) to ensure that the data being collected is accurate and audit-ready.

  • Vigilance & Reporting: Track and follow up on Serious Adverse Events (SAEs) with a strong understanding of global and local reporting requirements.

  • Strategic Support: Assist with investigator recruitment, regulatory submissions, and feasibility studies while providing back-office support for the sponsor’s broader clinical objectives.

  • Mentorship: Support the training and mentoring of new team members, contributing to a high-performing culture within the sponsor-dedicated team.

Candidate Profile: Requirements for Clinical Research Associate Job

This Life Sciences Job is tailored for professionals who have already built a strong foundation in independent monitoring and are ready for the complexities of sponsor-dedicated work.

  • Educational Background: A university degree in Life Sciences is mandatory to provide the necessary clinical and scientific context for monitoring.
  • Professional Experience: A minimum of 2 years of independent monitoring experience within a Pharma or CRO environment, specifically focused on interventional trials.
  • Therapeutic Expertise: While not mandatory, Oncology experience is a significant advantage, or at minimum, a strong willingness to specialize in complex oncological protocols.
  • Linguistic Skills: Proficiency in both English and Polish is essential for navigating local regulatory landscapes while collaborating on international studies.
  • Analytical Mindset: Strong knowledge of SAE reporting and the ability to exercise professional judgment in resolving complex site queries.

In summary, the Clinical Research Associate Job at Fortrea offers a unique blend of deep project ownership and global scale. By choosing a Fortrea career in 2026, you position yourself at the center of the industry’s most sophisticated FSP model, gaining the therapeutic expertise that only comes from dedicated sponsor work. Whether you are conducting on-site visits or managing remote queries, your work in this Life Sciences Job ensures that the next generation of medicines is brought to market with the highest quality and scientific integrity. If you are ready to own your professional journey and work with a team that values your growth, Fortrea Warsaw is where your ambition meets its match.

APPLY ONLINE HERE

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