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From the employer's careers site First seen 27 Oct 2026

Experimented CRA France - single sponsor

Syneos Health senior full-time

The employer hasn't listed a salary.

Apply on Syneos Health

Description

Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. The role of Experimented CRA France - single sponsor involves conducting on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.

Job Responsibilities

  • Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms
  • Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates
  • Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials
  • Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues
  • Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans
  • Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct

Qualifications:

  • Bachelor's degree in a related field or equivalent experience
  • Minimum of 2-4 years of experience in clinical research monitoring
  • Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements
  • Excellent communication and interpersonal skills
  • Ability to work independently and manage multiple priorities
  • Proficiency in using clinical trial management systems and other relevant software

Certifications:

  • Certified Clinical Research Associate (CCRA) or equivalent certification preferred

Necessary Skills:

  • Attention to detail and strong analytical skills
  • Problem-solving abilities and critical thinking
  • Ability to work effectively in a team environment
  • Strong organizational and time management skills
  • Proficiency in Microsoft Office Suite

Skills

Required

  • Good Clinical Practice (GCP)
  • clinical research monitoring
  • clinical trial management systems
  • Microsoft Office Suite

Nice to have

  • Certified Clinical Research Associate (CCRA)
Apply on Syneos Health