Site Documents Jobs in Poland

This position will support and observe clinical site monitoring services inhouse and provide monitoring and site management activities for full-service studies assessing for protocol SOP and regulatory compliance. Responsibilities include site management activities to help drive investigative sites...

Working with UsChallenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthrou...

IQVIA is hiring Associate Clinical Research Associates!Join IQVIA today and make an impact on patients outcome!Job OverviewEngage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol standard operat...

Job OverviewUnder general supervision perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include main...

Senior Site Feasibility Specialist IQVIA BiotechLocation: PolandWork Model: HomebasedEmployment Type: Full-timeAbout the RoleIQVIA Biotech is seeking a Senior Site Feasibility Specialist to support our growing clinical operations this role you will lead country-level Site Activation (SA) activitie...

Study Start-Up Specialist / Regulatory & Start-Up SpecialistIQVIA BiotechPoland HomebasedAt IQVIA Biotech we partner with visionary biotech companies to transform innovation into patient impact. With dedicated teams deep therapeutic expertise and a biotech-tailored delivery model we accelerate clini...