Start-up & Regulatory Specialist Ii

2 semanas atrás

São Paulo, Brasil Fortrea Tempo inteiro
**Shape the Future of Global Clinical Trials**
Join our dynamic team and lead the crucial start-up phase of impactful clinical trials, with opportunities for international exposure. You'll ensure projects are delivered on time, within budget, and to the highest quality standards, directly contributing to life-changing medical advancements.
**Your Impact**:
- Drive the development and execution of efficient start-up processes.
- Spearhead site-related start-up activities, ensuring seamless initiation.
- Collaborate with clients and internal teams, presenting at key meetings.
- Manage timelines, budgets, and documentation with meticulous accuracy.
- Ensure regulatory compliance and adherence to the highest ethical standards.
**Your Expertise**:
- Strong clinical research background (4+ years), including proven previous experience with study start-up projects.
- In-depth knowledge of ICH-GCP guidelines and international regulations (US FDA, MHRA).
- Excellent communication, leadership, and organizational abilities.
- Proven ability to manage multiple priorities and inspire teamwork in a virtual environment.
- Fluency in English and the local language.
Learn more about our EEO & Accommodations request here.

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