Resultados da pesquisa
- FortreaOeiras·
- You’ll also enjoy flexible work arrangements and the chance to make a meaningful impact in cutting-edge clinical research.
- IQVIAOeiras·
- Performing site selection, initiation, monitoring and close-out visits.
- Supporting the development of a subject recruitment plan.
- Driver’s license class B.
- Ver todas as Ofertas de emprego de IQVIA – ofertas para Oeiras – Ofertas de emprego de Senior Clinical Research Associate em Oeiras
- Pesquisa por salário: salários de Senior Clinical Research Associate - based in Portugal
- Consulte as perguntas e respostas sobre a empresa IQVIA mais populares.
- ICON PlcLisboa·
- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP.
- Extensive experience as a Clinical Research Associate,…
- Ver todas as Ofertas de emprego de ICON Plc – ofertas para Lisboa – Ofertas de emprego de Senior Clinical Research Associate em Lisboa
- Pesquisa por salário: salários de Senior CRA / CRA II
- AmgenLisboa·
- Hands-on experience implementing security for AI/ML systems used in clinical research, genomics, drug discovery, diagnostics, or digital health.
- AmgenLisboa·
- Hands-on experience implementing security for AI/ML systems used in clinical research, genomics, drug discovery, diagnostics, or digital health.
Job Post Details
Senior Clinical Research Associate - FSO Team - job post
Dados da oferta
Tipo de oferta
- Período Integral
Localização
Descrição Completa da Oferta
Join Fortrea as a SR Clinical Research Associate – Drive Clinical Excellence in Oncology Trials. This role is for upcoming future opportunities that may arise at Fortrea.
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:
3+ years of clinical monitoring experience, including Oncology therapeutic areas.
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!
micol.iafrate@fortrea.com
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