Clinical Research Associate Ii

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Join Fortrea as a Clinical Research Associate - Drive Clinical Excellence in Oncology Trials.

As a CRA II, 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**:

- 2+ years of clinical monitoring experience, specifically oncology 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**:

- 1+ 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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**Fortrea is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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