11 дней назад
Site Activation Specialist - Portugal
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Site Activation Specialist - Portugal (Clinical Trial Start-Up): Supporting country-level clinical trial start-up and site management in Portugal with an accent on feasibility, site identification, regulatory submissions, and site activation. Focus on managing essential documentation, coordinating contract and budget processes, and monitoring activation progress in compliance with ICH-GCP and local regulations.
Location: Portugal (home-based); based in Portugal required
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Act as the primary point of contact for assigned investigative sites.
- Execute feasibility, site identification, and site activation activities according to SOPs, regulations, and project timelines.
- Prepare, review, and manage essential site and regulatory documents.
- Support contract and budget processes with internal stakeholders.
- Maintain tracking tools, timelines, and internal systems with accurate project data.
- Monitor site activation progress and performance metrics while coordinating with Site Activation Managers, Project Management, and cross-functional teams.
Requirements
- Based in Portugal with a strong understanding of the local regulatory environment.
- 2–3+ years of experience in site activation, study start-up, or clinical research.
- Bachelor’s degree in Life Sciences or a related field.
- Knowledge of clinical trial start-up processes and regulatory requirements, including ICH-GCP.
- Experience managing site documentation and submission processes, with strong attention to detail and the ability to manage multiple sites and timelines.
- Fluent Portuguese and English, written and spoken.
Culture & Benefits
- Freelance, home-based engagement with a 0.5–0.75 FTE commitment.
- Immediate start.
- Approximately four-month engagement.
- Work focused on improving the development and commercialization of medical treatments and patient outcomes.
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