Lead Clinical Trial Operations Manager Jobs in Poland

Clinical Trial Psych Rater - Polish SpeakingLocation: Remote/VirtualHours: Estimated 1016 hours per monthRole: Clinical SpecialistAbout IQVIAIQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated to driving healthcare forward. We partner with the...

As the Manager of the Analytical Support Hub in Warsaw you will lead a newly established team that provides centralized analytical support to multiple Western European markets. Your role is pivotal in ensuring operational excellence and fostering collaboration across countries and internal NIQ teams...

Clinical Trial Educators (CTEs) collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimize the site experience and performance. They lead relat...

Therapeutic area: Hematology.Territorial scope (districts): zachodniopomorskie pomorskie lubuskie wielkopolskie kujawsko-pomorskie.The Medical Science Liaison (MSL) is a non-promotional field based scientific expert in a given therapeutic area(s) that strategically supports the medical and scientifi...

Job DescriptionJoin Our Award-Winning Biopharmaceutical Company!Position Overview:We are looking for a Medical Affairs Manager (MAM) to manage medical activities within one or more therapeutic areas under the guidance of the Medical Director/TA Lead.The MAM will collaborate among others with marketi...

GT was founded in 2019 by a former Apple Nest and Google executive.GTs mission is to connect the worlds best talent with product careers offered by high-growth companies in the UK USA Canada Germany and the Netherlands.On behalf ofAAVantgarde Bio GT is looking for an Expert Statistician interested i...

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. This is a sponsor facing role.Essential FunctionsOverse...

This position ensures that clinical study registrations and results are accurately routed tracked and entered into appropriate databases as per regulatory requirements and in line with Alexion principles policies and standards. This role will work globally with individual study teams to deliver reda...

This position is responsible for patient-facing materials delivery as required by EU Clinical Trial Regulation (EU CTR 536/2014) and Alexion public commitments to all participants taking part in Alexion-sponsored clinical trials. This role may also perform other CTT-related duties as assigned by lin...

This position is accountable for working autonomously and globally with systems and process owners business areas the Data Privacy Office and vendors to design implement and refine industry-leading methodology for automated clinical data and document anonymization and data privacy protection. This i...

Role OverviewThe Area Medical Director is accountable for setting and executing thearea-level medical affairs strategyacross multiple markets with a focus onrare and orphan diseases. This role aligns area priorities with Global Medical Affairs (GMA) and regional objectives identifies and addresses g...

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...

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...

As part of the PSI team you will have a fair degree of ownership and autonomy to make nuanced country-and department-specific adjustments while nurturing the global PSI culture that unites us across six continents. You will:Act as a specialized liaison to assist sites with a protocol-tailored approa...

Responsibilities Ensure consistent processes and efficient review of critical clinical/safety data Review of patient-level clinical/safety data on an ongoing basis to ensure medical accuracy and completeness coding consistency and generate applicable queries as needed to obtain information for appro...

At PrimeVigilance PV Officers are independent case processing team members who are expected to manage a variety of case processing services with full accountability.  If you join PrimeVigilance you can expect to work with teams of different sizes from small clinical trial to large generic post-marke...

Therapeutic area: Immunology.This position covers operations across the entire country.Preferred candidates locations: Central Poland (Warszawa Łódź).The pipeline Medical Science Liaison (pMSL) is a field-based scientific expert dedicated to facilitating scientific dialogue and supporting the scient...