Global Site Activation Manager
5.0
Töötajate arv: 20–50
Põhitegevusala: Teadus- ja arendustegevus loodus- ja tehnikateaduste vallas
Palk täpsustamataTuruvahemik: 1600–2450 €
Responsibilities
Leading global site activation activities across clinical trials, including site identification, feasibility, regulatory and ethics submissions, site contracting, protocol amendments, and study start-up timelines. Developing and executing site activation plans, managing regulatory documentation and risks, and coordinating with sponsors, sites, and cross-functional stakeholders.
Requirements
- Life Sciences degree
- Site activation experience
- Study start-up experience
- ICH-GCP knowledge
- Clinical trial regulations
- Regulatory affairs experience
- Protocol amendments
- Budget and timeline management
- Stakeholder management
- Cross-cultural experience
Employer offers
- Remote work
- Flexible working environment
- Structured career development
- Tailored training
- Mentorship
- AI-enabled technologies