CRA II Senior CRA
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Job Location:
Monthly Salary:
Posted on:
2 days ago
Vacancies:
1 Vacancy
Job Summary
Clinical Research Associate in Latvia
Future Opportunities Fixed Term & Permanent Roles
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 fixedterm 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 ICHGCP 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 crossfunctional teams.
Key Responsibilities
- Perform site monitoring activities including qualification initiation routine monitoring and closeout 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 comonitoring and knowledge sharing
- Travel is required (approximately 6080%)
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 ICHGCP 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 drivers license
What We Offer
- Opportunities to work on global clinical trials
- Collaborative and supportive team environment
- Competitive compensation and benefits
Learn more about our EEO & Accommodations request here.
Required Experience:
Senior IC
