Clinical Trials Jobs in Warsaw

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...

Fortrea is looking for a Clinical Data Scientist - R Programmer to join our team in Poland in a fully remote setup.In this role you will support Centralized Monitoring by configuring and maintaining systems setting up new studies and developing standard and bespoke monitoring functionalities. You wi...

Location: Warsaw PolandHybrid model of work: 3 days in office 2 remote per weekThe Global Clinical Supply Chain function is accountable for the supply of medicines to AstraZenecas clinical trials across the world. Our companys portfolio of emerging new medicines means the portfolio of clinical trial...

At Alcon were passionate about enhancing sight and helping people see brilliantly. With more than 25000 associates we innovate fearlessly champion progress and act swiftly to impact global eye health. We foster an inclusive culture recognizing your contributions and offering opportunities to grow yo...

Ergomed is looking for a freelance clinical project manager who is fluent in Mandarin and has early phase oncology experience to support bid defense activities initially on a 30 hours per month contract. The contract hours will increase once work is awarded.Bid defense activities initiallyServe as p...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Manager Clinical Admin 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 countri...

Senior Clinical Data Visualization Developer will be responsible for supporting mediumcomplexity data visualization mapping and setup activities across clinical programs. The role requires strong technical expertise independent problemsolving and the ability to translate business needs into clear a...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Manager - Make an Impact at the Forefront of InnovationThe Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specifi...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin us as an Associate Manager Sites And lead a team in overseeing site-based clinical research ensuring compliance with protocols managing staff optimizing site operations and driving the success of our clinical trials an...

Use Your Power for PurposeAt Pfizer our Worldwide Medical and Safety colleagues are pivotal in bridging evidence-based medical decision support with stakeholders to enhance health and treatment outcomes. Whether you are developing frameworks to ensure our evidence is scientifically robust offering u...

The Trial Delivery Leader (TDL) serves as the single point of accountability for trial operational strategy trial-level budget quality and on-time delivery of assigned clinical trials. This role represents the evolution of the Global Trial Leader (GTL) with a stronger emphasis on strategic leadershi...

At Roche you can show up as yourself embraced for the unique qualities you bring. Our culture encourages personal expression open dialogue and genuine connections where you are valued accepted and respected for who you are allowing you to thrive both personally and professionally. This is how we aim...

For the Client:To review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/expectedness an...

Pharmacovigilance Lead Signal Detection SummaryThe Pharmacovigilance Lead Signal Detection is a senior expert responsible for leading and executing signal detection and evaluation activities across assigned client portfolios. The role combines scientific and epidemiological expertise with operationa...

Pharmacovigilance Manager Benefit RiskPosition Summary The Pharmacovigilance (PV) Manager Benefit Risk is a senior safety professional responsible for leading and overseeing benefit-risk evaluation activities across assigned products and client portfolios. This role ensures the continuous assessme...

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...

Title: Logistics Coordinator Temperature-Control and MonitoringLocation: WarsawHybrid Model: 3 days per week from officeAt AstraZeneca every medicine we deliver starts with a reliable expertly managed supply chain. Our Clinical Manufacturing & Supply (CM&S) organisation ensures that investigational...

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...

For the Client:To review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/expectedness an...