CRA Job Opportunity at Fortrea | Apply Now
Looking for a rewarding CRA job in a global clinical research organization? This opportunity with Fortrea offers a dynamic remote role based in the Netherlands, where you can contribute to impactful clinical trials and advance your career in life sciences. If you’re passionate about patient safety, data integrity, and innovation, this role is designed for you.
- Job Title: Clinical Research Associate (CRA I)
- Location: Remote locations – Leiden, Remote Netherlands
- Time Type: Full Time
- Job Requisition ID: 26380
About the Company
CRA job opportunities at Fortrea provide access to a globally recognized clinical research organization dedicated to advancing healthcare innovation. Fortrea specializes in supporting clinical trials and improving patient outcomes through cutting-edge research and collaborative expertise. Known for its inclusive culture and global presence, Fortrea careers offer strong professional growth and learning opportunities.
Job Description
CRA job role involves working as a Clinical Research Associate (CRA I) responsible for supporting and executing clinical studies. This remote job based in the Netherlands focuses on ensuring clinical trials are conducted efficiently while maintaining compliance with regulatory standards and protocols.
Qualifications
CRA job requirements include:
- University degree in a related life sciences or health field, or equivalent relevant experience.
- Basic knowledge of regulatory guidelines and clinical trial processes.
- Fluency in English and the local office language (Dutch for NL, Dutch and French for BE).
- At least 6 months of independent monitoring experience.
- Strong organization, planning, and problem-solving skills.
- Proficiency with standard computer applications.
- Ability to work effectively in a matrix environment.
- Valid driver’s license.
Key Responsibilities
CRA job responsibilities include:
- You will conduct all aspects of study site monitoring, including routine visits, initiation, and close-out activities.
- You will oversee site management activities in alignment with project plans and SOPs.
- You will ensure study staff are properly trained and equipped to conduct the protocol safely and accurately.
- You will safeguard patient safety by verifying informed consent and adherence to protocol and regulatory requirements.
- You will review source documentation to ensure data integrity and identify missing or inconsistent data.
- You will manage monitoring tasks efficiently and in line with Fortrea policies, including economical travel planning.
- You will maintain audit-ready site documentation.
- You will prepare clear and timely monitoring visit reports.
- You will collaborate with internal teams to assess project needs, timelines, and resources.
- You will act as a point of contact for clinical trial supplies and assigned vendors.
- You will participate in feasibility assessments, QC visits, and registry management tasks.
- You will support activities such as investigator recruitment, EC submissions, regulatory notifications, and meeting organization.
- You will follow up on Serious Adverse Events (SAEs), including report processing and narrative review.
- You will review CRFs, generate queries, and resolve data issues according to guidelines.
- You may mentor and co-monitor with new team members.
