Regulatory Guidelines Jobs in Poland

Make your mark for patientsWe are looking for aDigital Marketing Lead East Central Europe who is eager to join our Patient Impact Mid-Market department based inour site in Warsaw Poland.About the roleAs a Digital Marketing Lead East Central Europe (ECE) you will drive omnichannel campaigns based on...

Job OverviewDirect and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budget and resources.Essential FunctionsOversee the execution of Site Activat...

This is a remote position. As a Senior SAP EWM/LE Consultant you will join the supply chain and operations practice of our client a global management and technology consulting firm. The project focuses on driving an enterprise-scale S/4HANA logistics transformation for an international leader i...

Regulatory Reporting FRA Analyst Own and execute daily / monthly production of FR 2052a FRY14 FRY15 liquidity reports ensuring completeness accuracy and timeliness. Prepare and validate FDIC regulatory reports in compliance with 12 CFR 369 (FDIC reporting requirements) and 12 CFR 370 (recordkeeping...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Country Approval Specialist Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 co...

This is an exciting opportunityfor TMF Quality Project Manager (TMF Lead) role within Records Management department. If you are experienced in TMF management and cross functional collaboration you are motivated and have strong communication skills please review and apply!TMF Quality Project Manager...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as Director Clinical Operations Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 cou...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionDeadline for applications: June 5th 2026Join Us as Director Clinical Operations Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs span...

Use Your Power for PurposeWere looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your d...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Principal CM Analyst Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 countries...

Title:Public Affairs ManagerCompany:Ipsen Poland LLCAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience with global hubs...

Title:Patient Advocacy & Communication ManagerCompany:Ipsen Poland LLCAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology Rare Disease and Neuroscience. Supported by nearly 100 years of development experience...

Regulatory and Start Up SpecialistPoland - HomebasedFixed Term Contract Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and cont...

Internal Job DescriptionMake an impact on patient health!IQVIAs Global Site Activation Team of 2000 employees drives best in class site and customer experience with industry leading outcomes.We keep the patient at the forefront; Always Impatient for the Patient and we excel in our collaboration with...

Fortrea is looking for Senior Biostatistician to join our sponsor dedicated teamAs a Senior Biostatistician at Fortrea you will play a crucial role in the design analysis and interpretation of clinical trials directly impacting the development of innovative therapies and treatments. Supported by a d...

Job OverviewDirect and manage the delivery of all required site activation maintenance and regulatory activities for selected studies or multi-protocol programs including pre-award activities oversight of the scope of work budget and resources.Essential FunctionsOversee the execution of Site Activat...

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...

Study StartUp ManagerClinical Operations Regulatory & Site ActivationLocation: Flexible / officebased depending on project needsTravel: Occasional travel may be requiredContract Length: 3- 6 monthsAre you an experienced Regulatory & StartUp professional looking to lead complex clinical trial startu...

RESPONSIBILITIES Serve as primary point of contact for customer on data management deliverablesManage multiple large studies or program of studies (possibly global)Provide leadership and senior support to DTLs on multiple large global programs of global studiesProvide project management expertise wo...

Job OverviewManages a single department or work unit responsible for site activation. Sets goals and objectives for team members for achievement of short-term operational or tactical results. Essential FunctionsManages staffs delivery of site activation activities in accordance with organizations...