Job Description
Fortrea is currently seeking a pro-active Clinical Trial Administrator to join our expanding team in Drammen, Norway. For this particular role we are ideally looking for a ‘career’ clinical research administrator who does not wish to progress to a CRA or Project Management role.
This client-dedicated role is to be mainly office based in Drammen, Norway, and ideally you will have at least 2 years experience of supporting Clinical Trials.
Essential Job Duties:
- Act as contact for project team and study sites
- Perform CRF review against established data review guidelines, under direct supervision on management systems
- Assist with the management of study supplies and organize shipments
- Create, update, track, and maintain study-specific trial management files, tools, and systems.
- Assist the local project team members with other administrative activities as required (e.g. payments to investigators, correspondence with clients, preparation of status reports, and organization of investigators’ meetings)
- Coordinate meetings with clients, investigators, and project team, including taking minutes.
- Ensure compliance with Fortrea's SOPs, FDA, ICH, and GCP regulations for clinical conduct in all aspects of daily work
- Provide input in writing Monitoring Conventions as assigned
- Assist in submissions and notifications to Ethics Committees and Regulatory Authorities
Other Information: This role is a full time & permanent position to be employed through Fortrea.
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Did you know?
Labcorp's Clinical Development and Commercialization Services business is now Fortrea in connection with its planned spin-off from Labcorp, which is expected in mid-2023. Fortrea’s spin-off from Labcorp is subject to satisfaction of certain customary conditions. This spin-off will position both organizations for accelerated growth and allow each to focus resources on distinct strategic priorities, customer and employee needs and value creation opportunities. As a provider of phase I-IV clinical trial management, regulatory guidance, patient access solutions and market access consulting, Fortrea will partner with both emerging and large pharmaceutical, biotechnology, device and diagnostic companies to drive healthcare innovation and improve the lives of patients worldwide.
Fortrea is looking for problem-solvers and creative thinkers who are passionate about breaking down barriers faced by sponsors of clinical trials, and who are committed to helping transform the development process to get promising life-changing ideas and therapies to patients faster. Join us as we cultivate a workspace where all employees have the opportunity to grow and make impacts on a global scale. For more information and questions related to Fortrea, please visit www.fortrea.com.
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp 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. We encourage all to apply.
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