Sr. Clinical Research Associate (Hungary)

8 hours, 31 minutes 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/or perform full clinical site monitoring services for one or more projects.
  • Design and oversee project monitoring services, including training, site and patient recruitment, site data and document management, monitoring site budgets, and regulatory filings.
  • Act as the Lead CRA and primary liaison between CRAs and the project team.
  • Participate in the development of project plans, protocols, CRFs, communications, and other monitoring documents and tools.
  • Serve as a subject matter expert, mentor, and coach for peers, and provide performance feedback to management as needed.
  • Assist with selecting, hiring, training, supervising, and co-monitoring CRAs.
  • Resolve site and patient issues and address sponsor concerns as the first escalation point when required.
  • Represent leadership in business development initiatives focused on site monitoring.
  • Direct and guide day-to-day monitoring activities for groups of projects and review and approve monitoring reports.
  • Act as the primary clinical site contact and coordinate communication between sites, project teams, and sponsors.

Requirements

  • Minimum of a college diploma or degree.
  • 4-6 years of related experience.
  • Strong communication skills and a commitment to achieving positive results.
  • Strong attention to detail and the ability to build collaborative relationships.
  • Critical thinking abilities.
  • Ability to travel regularly to study sites approximately 5-8+ days per month, depending on project and business needs.
  • Home-based work arrangement.
  • Experience supporting complex and/or multinational clinical projects is preferred.
  • Ability to work within SOPs, study guidelines, and GCP best practices.

Benefits

  • Home-based working arrangement.
  • Regular travel to study sites as part of the role.

Interested in this position?

Apply directly on the company website

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