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CRA II​/Senior CRA

Job in Berkey, Lucas County, Ohio, 43504, USA
Listing for: Fortrea
Full Time position
Listed on 2026-06-28
Job specializations:
  • Research/Development
    Clinical Research
Job Description & How to Apply Below
Position: CRA II/ Senior CRA
Location: Berkey

Clinical Research Associate in Latvia

At Fortrea, we are building a pipeline of experienced CRA professionals for upcoming opportunities that may arise across our clinical programs. These opportunities may be offered on a fixed-term or permanent basis, depending on business needs.

The CRA II/ Senior CRA is responsible for site monitoring and site management activities in accordance with Fortrea and/or Sponsor SOPs, ICH-GCP, and applicable regulatory guidelines. The role supports the delivery of clinical trials by ensuring subject safety, data integrity, and protocol compliance, while contributing to project execution and collaboration within cross-functional teams.

Key Responsibilities
  • Perform site monitoring activities including qualification, initiation, routine monitoring, and close-out visits
  • Ensure protection of study participants and compliance with informed consent, protocol, and regulatory requirements
  • Review source data and CRFs to ensure data accuracy, completeness, and integrity
  • Manage site relationships and ensure audit readiness at the site level
  • Prepare accurate and timely monitoring visit reports
  • Track and follow up on Serious Adverse Events (SAEs)
  • Support project activities, including feasibility, investigator meetings, and vendor collaboration
  • May act as Lead CRA or Local Project Coordinator on assigned studies
  • Mentor junior staff through co-monitoring and knowledge sharing
  • Travel is required (approximately 60–80%)
Qualifications & Experience
  • University degree in life sciences or related field, or equivalent clinical research experience
  • Minimum 2- 3 years of clinical monitoring experience in a CRO or pharmaceutical environment
  • Strong knowledge of ICH-GCP, regulatory requirements, and drug development processes
  • Advanced site monitoring and site management skills
  • Fluency in English and local language (written and verbal)
  • Ability to work independently in a matrix environment
  • Valid driver's license
What We Offer
  • Opportunities to work on global clinical trials
  • Collaborative and supportive team environment
  • Competitive compensation and benefits
Position Requirements
10+ Years work experience
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