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You will be part of a bespoke and highly skilled statistical programming team working to the most up to data quality standards. You will work closely with other members of the Biostatistics and DM departments on various clinical projects and may act as Lead Statistical Programmer on multiple projects.
- Manage or lead assignments and programming personnel on single or multiple projects
- Mentor and train selected associates within the Statistical Programming group
- Participates in the development of and ensures compliance to SOPs, policies, and guidelines
Publicerad 14 augusti
inVentiv Health Clinical, Stockholm
As a CTA you would administer, maintain and co-ordinate the logistical aspects of clinical trials in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs) covering Denmark, Norway, Finland and Sweden.
- To handle all study related administrative tasks by utilizing technology effectively to support the clinical trial development processes with the use of Clinical Trial Management System at the Protocol, Country and Site level.
- Ensure that any clinical trial databases/tracking tools are set up and maintained throughout the trial
- Collaborate with the study project team to reach target within set timelines
Publicerad 10 augusti
Läkemedelsföretaget Sobi som framställer biologiska läkemedel söker nu dig som har djupa kunskaper inom GMP och specifikt omgivningshygien...
Academic Work, Stockholm
Academic Work, 17 augusti
Socialförvaltningen Är du Sveriges bästa socionom?
Uppsala kommun, Uppsala
Platsbanken AMV, 16 augusti