CRA II/ Senior CRA

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 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 Learn more about our EEO & Accommodations request here .