Clinical Research Associate Jobs at Fortrea, Latvia | Life Sciences | Apply Now
A rare chance has emerged for professionals seeking clinical research associate jobs at Fortrea in Vilnius. This role is ideal for individuals with a background in life sciences clinical research who are eager to enhance their skills in a supportive environment. Applications are welcomed from qualified candidates ready to contribute to impactful clinical trials.
- Job Position: Clinical Research Associate I – FSO
- Location: Riga, Latvia
- Job Requisition ID: 264282
About The Company
Fortrea is a leading organization in the life sciences sector, specializing in clinical research and development. The company is dedicated to advancing healthcare by conducting clinical trials across various therapeutic areas. With a commitment to quality and innovation, Fortrea provides a dynamic environment for professionals to grow their careers while making significant contributions to patient care.
Job Description
The Clinical Research Associate position at Fortrea involves supporting the successful delivery of clinical trials. Candidates will contribute to the execution of clinical studies across a variety of therapeutic areas, including Oncology, Dermatology, Respiratory, Cardiology, and Diabetes. This role is suited for professionals with at least two years of onsite monitoring experience, looking to develop their monitoring skills in a structured environment.
Clinical Research Associate Jobs – Key Responsibilities
- Support the management of clinical trial sites in compliance with Fortrea SOPs, ICH-GCP, study protocols, and sponsor requirements, with appropriate supervision.
- Assist in the preparation and conduct of site monitoring activities, including site initiation, routine monitoring, and close-out visits, ensuring patient safety and protocol adherence.
- Perform source data verification (SDV), support query resolution, and review eCRFs to help ensure data quality and completeness.
- Maintain and update essential trial documentation: in eTMF and sponsor systems to support inspection readiness.
- Support investigational product (IP)Â tracking and accountability checks in collaboration with the study team.
- Collaborate with cross-functional teams and escalate issues appropriately, contributing to site performance, quality, and timelines.
Eligibility Criteria Required For Clinical Research Associate Jobs
- University or college degree in life sciences, nursing, pharmacy, or a related field; relevant internships or equivalent experience will be considered.
- Minimum of 2 years of onsite monitoring experience.
- Basic understanding of ICH-GCP guidelines: and clinical trial processes.
- Strong attention to detail, willingness to learn, and ability to follow established procedures and documentation standards.
- Fluency in English, both written and spoken.
- Comfortable using clinical systems and tools, with openness to travel as required for site visits.
Why Join Fortrea?
- Grow your clinical research career in a structured and supportive environment: with clear development pathways and mentoring.
- Gain hands-on exposure to global clinical trials and multiple therapeutic areas while building strong foundational CRA skills.
- Benefit from formal training programs, modern clinical systems, and continuous learning opportunities.
- Enjoy a flexible work model, competitive benefits, and a culture that values collaboration, quality, and well-being.
If you are curious, detail-oriented, and eager to make an impact on patients’ lives, Fortrea encourages you to apply.
The opportunity to secure clinical research associate jobs at Fortrea is now available for qualified candidates. This role offers a unique chance to engage in life sciences clinical research while contributing to meaningful clinical trials. Interested individuals are encouraged to apply at the earliest to be part of a team that values expertise and dedication.
Biotecnika is a career information portal. Please verify all details from the original notification before applying.
