Lead CRA: Site Monitoring & Start-Up

BELGIUM

Belgique

Hybride

EUR 45 000 - 72 000

Plein temps

14 jours+

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Avantages offerts par ce poste

Hybrid work from home
Health benefits
Paid parental leave

Résumé du poste

CTI Clinical Trial and Consulting Services is seeking a Clinical Research Associate to monitor trials, manage site visits, and drive start-up activities. You will ensure regulatory compliance, oversee IP/material handling, and collaborate across sponsor and project teams.

The role requires 3+ years in clinical trial monitoring, a relevant degree, and strong communication. CTI offers hybrid work options, competitive benefits, and opportunities to advance in a global CRO.

Qualifications

  • 3+ years of clinical trial monitoring experience or equivalent
  • Bachelor's degree or higher in allied health such as nursing, pharmacy, health/natural science, or RN with associates degree, or 3-year Nursing Diploma with at least 2 years nursing experience
  • Experience in conducting clinical research studies in hospital, pharma, or CRA environments

Responsabilités

  • Serve as main CTI contact for assigned study sites
  • Conduct site visits (PSV, SIV, IMV, COV) and complete visit deliverables
  • Assist with study start-up activities including feasibility and site selection
  • Collect, review and track essential regulatory documents
  • Provide ongoing updates to Sponsor/Client and participate in meetings
  • Lead CRAs and mentor junior team members
  • Liaise with Data Management for data cleaning activities
  • Identify and propose process improvements

Connaissances

Clinical trial monitoring
Regulatory knowledge
Team leadership
Documentation accuracy

Formation

Bachelor's degree

Description du poste

CTI Clinical Trial and Consulting Services is seeking a Clinical Research Associate to monitor trials, manage site visits, and drive start-up activities. You will ensure regulatory compliance, oversee IP/material handling, and collaborate across sponsor and project teams.

The role requires 3+ years in clinical trial monitoring, a relevant degree, and strong communication. CTI offers hybrid work options, competitive benefits, and opportunities to advance in a global CRO.

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