Sr. Clinical Research Associate

1 hour, 12 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 and deliver full clinical site monitoring services for one or more projects, including complex and multinational studies.
  • Design and oversee project monitoring services in alignment with SOPs, study guidelines, and GCP best practices.
  • Support site and patient recruitment, site data and document management, monitoring budgets, and regulatory filings.
  • Act as Lead CRA and primary liaison between CRAs and the project team on assigned studies.
  • Participate in the development of project plans, protocols, CRFs, communications, and other monitoring tools when required.
  • Serve as subject matter expert, mentor, coach, and performance feedback resource for peer CRAs.
  • Assist with selection, hiring, training, supervision, and co-monitoring of CRAs as needed.
  • Act as the first escalation point for site and patient issues or sponsor concerns when required.
  • Lead or participate in study team, kickoff, and investigator meetings and serve as a sponsor contact for monitoring-related issues.
  • Identify and recruit site investigators, coordinate trial materials and investigational product delivery, and support investigational site setup.

Requirements

  • College diploma or degree.
  • 4-6 years of related experience.
  • Strong communication skills and self-motivation.
  • Strong attention to detail and commitment to achieving positive results.
  • Critical thinking abilities.
  • Ability to build collaborative relationships with stakeholders.
  • Ability to regularly travel to sites.
  • Home-based/remote work arrangement.
  • Experience in clinical site monitoring or related clinical research work is implied.
  • Experience with site recruitment, regulatory filings, CRFs, or monitoring tools is preferred based on role scope.

Benefits

  • Home-based, remote working arrangement.
  • Regular travel required as part of the role.
  • Full-time, permanent employment.

Interested in this position?

Apply directly on the company website

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