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Start-up - Regulatory Specialist II
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Esta es una vacante externa, deberás completar el proceso en el sitio de la empresa.
Sobre el empleo
Categoría: Sector salud
Subcategoría: Farmacéutica
Educación mínima requerida:
Detalles
Horario:
Tiempo completoEspacio de trabajo:
PresencialDescripción
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.
Ready to make a difference? Apply now!
Learn more about our EEO & Accommodations request here.
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.
Ready to make a difference? Apply now!
Learn more about our EEO & Accommodations request here.
Recuerda que ningún reclutador puede pedirte dinero a cambio de una entrevista o un puesto. Asimismo, evita realizar pagos o compartir información financiera con las empresas.
ID: 20502180
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