Clinical Trial Administrator, Havneholmen
- Employer
- Labcorp
- Location
- Copenhagen, Hovedstaden (DK)
- Salary
- Competitive with great benefits
- Start date
- 14 Mar 2019
- Closing date
- 13 Apr 2019
View more
- Discipline
- Clinical Research, Clinical Administrator, Clinical Research Associate, Clinical Research Nurse, Study Site Coordinator
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Covance is currently seeking a pro-active Clinical Trial Administrator to join our expanding team in Copenhaguen. For this particular role we are ideally looking for a ‘career’ clinical administrator who does not wish to progress to a CRA or Project Management role.
This client-dedicated role is to be office based in Havneholmen. Copenhaguen and ideally you will have at least 2 years experience of supporting Clinical Trials in Denmark. Much of the work will involve complex Oncological Clinical Trials and so there is plenty of interesting (and worth while) work to get your teeth stuck into!
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 Covance 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
This role is a full time & permanent position to be employed through Covance, sponsor dedicated: you will be working only with the clinical trials of one sponsor and only one set of SOPs!
Education - Qualifications
- University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
- In lieu of the above requirement, candidates proven relevant clinical research experience in pharmaceutical or CRO industries will be considered
Experience
Experience in supporting Clinical Trials in Denmark is needed, ideally min. 2 years in international ph I-III studies.
Experienced windows user familiar with: Excel, Word, Powerpoint, OneNote, Outlook.
Able to manage and deal with big amounts of data /numbers (knows how to use the Windows programs for the tasks) and organize reports and lists to make them manageable and presentable.
Structured and organized – in combination with enjoying unforeseen tasks and challenges.
Comfortable even though there is no answer key to many tasks.
Comfortable with routine tasks also.
Able to work independently and proactively.
Company
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.
- Website
- https://careers.labcorp.com/global/en
- Location
-
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
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