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