Sr. Clinical Research Associate (Netherlands)

2 months ago
Full-time
Senior
Project and Program Management
Alimentiv

Alimentiv

Alimentiv specializes in providing comprehensive clinical research services for gastrointestinal and liver diseases, leveraging a global site network, advanced medical imaging, and biomarker discovery to enhance patient recruitment and accelerate clini...

Professional Services
251-1K
Founded 1986

Description

  • Manage, deliver, and perform full clinical site monitoring services for one or more projects.
  • Oversee the design and execution of monitoring services, including training, site/patient recruitment, data and document management, monitoring budgets, and regulatory filings.
  • Act as the primary liaison between CRAs and the project team in the Lead CRA role.
  • Participate in the development of project plans, protocols, CRFs, communications, and other monitoring tools and documents.
  • Serve as a subject matter expert, mentor, coach, and source of performance feedback for peers.
  • Assist with selecting, hiring, training, and supervising CRAs as needed.
  • Conduct co-monitoring and training visits with CRAs.
  • Act as the first escalation point for site/patient issues or Sponsor concerns when required.
  • Lead or support monitoring services for groups of projects and/or CRAs on large or complex studies.
  • Represent the organization in study team, kickoff, investigator meetings, and business development initiatives focused on site monitoring.

Requirements

  • College diploma or degree is required.
  • 4–6 years of related experience is required.
  • Strong communication skills are required.
  • Strong attention to detail is required.
  • Critical thinking abilities are required.
  • Self-motivation and a commitment to achieving positive results are required.
  • Ability to build collaborative relationships with stakeholders is required.
  • Ability to regularly travel to study sites approximately 5–8+ days per month is required, depending on project and business needs.
  • Home-based work arrangement is required.
  • Experience in clinical site monitoring, CRA leadership, or related clinical research functions is preferred.

Interested in this position?

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