Clinical Research Associate
4 weken geleden
As a leading global contract research organization (CRO), Fortrea is seeking a talented Clinical Research Associate to join our team in the Netherlands. The successful candidate will be responsible for all aspects of study site monitoring, including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, and liaison with vendors.
Key Responsibilities:
- Responsible for all aspects of study site monitoring, including routine monitoring and close-out of clinical sites
- Maintenance of study files, conduct of pre-study and initiation visits
- Liaison with vendors
- General On-Site Monitoring Responsibilities:
- Assist Senior CRAs and CRA-2 with on-site tasks as required and according to training goals
- Initiate, monitor and close out clinical investigative sites, with or without direct supervision from Senior Clinical Research Associates, Clinical Team Leads, Project Managers or Project Directors
Requirements:
- Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
- Minimum 1 year of direct monitoring experience
- Excellent understanding of Serious Adverse Event (SAE) reporting
- Ability to resolve project-related problems and prioritize workload for self and team
- Fluent Dutch and English
Fortrea is committed to revolutionizing the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. We are seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials.
Fortrea is an Equal Opportunity Employer:
As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic.
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