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CTA / Senior Clinical Trial Administrator - Sweden (Stockholm)

Employer
Labcorp
Location
Danderyd, Sweden
Salary
Competitive
Start date
6 Jan 2021
Closing date
4 Feb 2021

View more

Discipline
Finance / Administration, Administration
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details


Covance is currently seeking a pro-active Clinical Research Assistant to join our expanding team inStockholm. This is a client-dedicated role to be office based in Stockholm and ideally you will have at least 1-2 years experience of supporting Clinical Trials in Sweden. 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, query generation and resolution against established data review guidelines, under direct supervision on management systems
  • Assist with generation and reconciliation of queries to investigative sites/clients to resolve problem data
  • 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
  • General On-Site Monitoring Responsibilities:
    • Assist Senior CRAs, CRA-2 and CRA-1 with on-site tasks as required and according to training goals (e.g. review of Case Report Forms and Study File Notebook, drug accountability)


Other Information: This role is afull time & permanent position to beemployed through Covance. For more information please contact Andy Smith at Covance on +44 (0)7775 848 250 or mail andy.smith@covance.com

Key words: CTA, Clinical Trial Administrator Sweden, Stockholm, GCP, CRO, Pharmaceutical, Clinical Administration Sweden CTA, Oncology
Education/Qualifications:
A degree ideally but not essential
Experience:
1-2 years in Clinical Trials in Sweden

Fluency in Swedish (essential)

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.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom

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