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In-house CRA I/ In-house CRA II

2 hours, 22 minutes ago
France
Full-time
Entry Level
Project Coordinator
Project and Program Management
Apply Now
Precision For Medicine

Precision For Medicine

Precision for Medicine is a specialized scientific services company that helps pharmaceutical and life sciences clients innovate, develop, and commercialize next-generation medical products. With a diverse team of experts, they offer comprehensive serv...

Pharmaceuticals
1K-5K
Founded 2012
$225M raised
View All Jobs 52

Description

  • Assist with investigator recruitment and site feasibility activities using study materials, questionnaires, and other evaluation tools.
  • Schedule internal and external meetings as needed.
  • Prepare and distribute Investigator Site Files to study sites, including coordination with shipping vendors when required.
  • Collect, review, maintain, and close out essential documents in the trial master file (TMF) to support sponsor and investigator compliance.
  • Set up and maintain site-related data in clinical systems, including tracking milestones and activities in the CTMS.
  • Serve as a site contact for study and site management issues, including answering questions, managing supplies, and escalating risks or issues.
  • Ensure timely and complete data entry by sites in EDC and other required systems.
  • Send study communications such as email updates, newsletters, and core document revisions to site personnel.
  • Support samples management, study supply management, investigational product accountability, and invoice follow-up for investigator payments.
  • Assist with data review, query resolution, database closure and freezing, and remote review of the electronic Investigator Site File where applicable.

Requirements

  • Bachelor’s degree or international equivalent, or an equivalent combination of education and experience, ideally in a business, scientific, or healthcare discipline.
  • Minimum of 1 year of relevant experience.
  • Location in Paris or the Paris area, France.
  • High proficiency in Microsoft Office applications, including Outlook, Word, Excel, and PowerPoint.
  • Fluency in French and English, both written and verbal.
  • Working knowledge of the drug development process.
  • Ability to travel as needed.
  • Solid experience in clinical research or related experience preferred.
  • Excellent organizational skills preferred.
  • Ability to work efficiently in a remote work environment preferred.

Benefits

  • Remote work environment flexibility.
  • Opportunity to work on clinical research studies across multiple sites and projects.
  • Chance to mentor a trainee In-house CRA, depending on assignment.
  • Equal opportunity employer status.
  • Reasonable accommodation support for applicants with disabilities.

Interested in this position?

Apply directly on the company website

Apply Now

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