Clinical Operations Associate — Remote 4 Days / Flexible Hours

CareForce One

Brussel

Ibrido

EUR 42.000 - 52.000

Tempo pieno

14 giorni+

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Vantaggi offerti da questo lavoro

Remote work up to 4 days per week
Collaborative team of ~40 colleagues
Real growth paths

Descrizione del lavoro

CareForce One is seeking a proactive Clinical Operations Assistant to join our trials team in Belgium. This role blends administrative rigor with site-facing collaboration to drive study progress and regulatory readiness.

You will manage TMF/CTMS documentation, support site activation, and coordinate with teams to resolve queries, audits, and monitoring preparations, all while maintaining high attention to detail and proactive communication.

Competenze

  • Bachelor’s or Master’s degree in Life Sciences (Biomedical, Pharmaceutical, etc.).
  • 1–2 years of professional experience in clinical research.
  • Proactive, independent and communicative with initiative.

Mansioni

  • Site Activation & Support: Collect, process, and file country- and site-specific documents required for regulatory submissions and site activation.
  • Proactive Site Engagement: Actively follow up with clinical sites, using phone to unblock delays and handle conversations.
  • Systems & Documentation: Maintain and update the TMF, CTMS, and other study tracking tools.
  • Study Lifecycle Support: Assist with sample and IMP kit reconciliation, resolve queries, and support monitoring visits and audits.
  • Process Improvement: Participate in expert task forces to optimize internal departmental workflows.

Conoscenze

Proactive mindset
Independent working
Excellent organization
Prioritization across tasks
Attention to detail

Formazione

Bachelor’s or Master’s degree in Life Sciences

Strumenti

TMF
CTMS

Descrizione del lavoro

CareForce One is seeking a proactive Clinical Operations Assistant to join our trials team in Belgium. This role blends administrative rigor with site-facing collaboration to drive study progress and regulatory readiness.

You will manage TMF/CTMS documentation, support site activation, and coordinate with teams to resolve queries, audits, and monitoring preparations, all while maintaining high attention to detail and proactive communication.

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