CTA / Senior Clinical Trial Administrator - Sweden (Stockholm)

Employer
Covance
Location
Stockholm, Stockholms län, Sweden
Salary
Competitive
Closing date
9 Oct 2020

View more

Discipline
Finance / Administration, Administration
Hours
Full Time
Contract Type
Permanent
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Job Overview:
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)

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Join our growing team and discover your extraordinary potential


We are recognized as a leader in drug development because of our exceptional people. At Covance, we embrace and celebrate the different strengths, experiences and perspectives of our 20,000+ team members across the globe. Our team is driven by an energizing purpose to improve health and improve lives. Here, you can play a role in bringing new scientific discoveries to life and make a difference in the lives of millions. And, our comprehensive service portfolio provides the opportunity to explore diverse projects and unique career paths across the drug development spectrum.

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Contact Us
  • Maidenhead Office Park
  • Westacott Way
  • Maidenhead
  • SL6 3QH
  • United Kingdom
  • Mini-site: Covance
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