SynteractHCR is an international CRO located in EU, RUS, US and South America. As we are growing we are looking for a dedicated CRA to join our Clinical Operations Team in Sweden. We offer you a challenging and rewarding job opportunity in a fast moving, flexible environment and a highly motivated team.
Responsible for the monitoring of clinical trials throughout Sweden and Finland and tracking study progress for our clients Interface with the SynteractHCR study team to ensure timely initiation and completion of clinical trials Collect study related data and assist with the preparation, review and submission of regulatory documents to regulatory authorities Contribute to the overall management of trials in accordance with ICH-GCP standards, local requirements and SOPs Start-up, maintenance and closure activities of clinical studies including the maintenance of the TMF and study documentation
Degree in life science 2+ years experience as a CRA Good scientific knowledge and understanding of clinical trials Good ICH-GCP knowledge and legal regulatory requirements Motivated, dedicated and service orientated approach Distinctive organizational skills, good time management and ability to meet deadlines Very good English and Swedish skills (verbal and written), a nice add on would be also Finnish skills, IT proficiency Willingness to travel
Have we sparked your interest? Then we are looking forward to receiving your application! Please apply through our homepage synteracthcr.com and state your earliest start date/notice period and your desired salary. If you have any questions regarding the position please contact antonia.schultzeynteracthcr.com