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Sr. Clinical Research Associate (Belgium)

1 month ago
Belgium
Full-time
Senior
Project Manager
Project and Program Management
Apply Now
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
View All Jobs 25

Description

  • Manage, deliver, and perform full clinical site monitoring services for one or more projects.
  • Oversee project monitoring services, including training, site and patient recruitment, site data and document management, monitoring site budgets, and regulatory filings.
  • Act as Lead CRA and primary liaison between CRAs and the project team.
  • Participate in the development of project plans, protocols, CRFs, communications, and other monitoring tools and documents.
  • Maintain collaborative relationships with stakeholders and represent the company in client and project interactions.
  • Act as subject matter expert, mentor, and coach for peers, and provide performance feedback to management as needed.
  • Assist with selection, hiring, training, and supervision of CRAs.
  • Conduct co-monitoring and training visits with CRAs and serve as first escalation point for site or sponsor issues when required.
  • Manage monitoring services for a group of projects and/or CRAs, including directing day-to-day activities and reviewing or approving monitoring reports.
  • Support site investigator identification and recruitment, site setup, trial materials delivery, and site communication throughout the project lifecycle.

Requirements

  • College diploma or degree.
  • 4-6 years of related clinical research experience.
  • Self-motivation and strong communication skills.
  • Strong attention to detail.
  • Critical thinking abilities.
  • Commitment to achieving positive results.
  • Ability to build collaborative relationships.
  • Ability to travel regularly to sites.
  • Home-based/remote working arrangement.
  • Experience with site monitoring, GCP, SOPs, and regulatory processes (implied by role responsibilities).

Benefits

  • Remote/home-based work arrangement.
  • Permanent full-time position.
  • Annual salary of €58,000 - €73,500.
  • Opportunity to work on complex and multinational clinical studies.
  • Regular travel to sites as part of the role.

Interested in this position?

Apply directly on the company website

Apply Now

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