PSI is a leading Contract Research Organization with more than 22 years of experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Safety reporting is incredibly important in the development of new medications. Join our global Pharmacovigilance team and address safety matters in an accurate and timely manner. You will build a career on the frontline of clinical research, while identifying risks associated with investigational products and ensuring better patient protection.
Home-Based or Offie-Based in
You will:Develop study-specific safety management plansSet-up and maintain project and product-specific safety databasesParticipate in the review and triage of incoming SAE reportsPrepare narratives for reportable adverse eventsBe a point of contact for investigative sites, clients, in-house project teams regarding safety informationSupport periodic safety reporting to regulatory agencies and address their questionsDevelop and implement training in safety aspects of clinical researchAssist in preparation for the audits and inspections in the matters of safety reporting
QualificationsUniversity degree in Life Sciences or PharmD or an equivalent combination of education, training & experiencePhD is a plusExperience in clinical or academic researchRelevant experience in safety reporting is a plusFull working proficiency in English and CzechPC skills to be able to work with MS Word, Excel and PowerPointAnalytical skills and ability to work with large amounts of informationCommunication and organizational skills
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
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