Przeglądaj w Polska · Warsaw · Asystent badań klinicznych
Asystent badań klinicznych w Warsaw
Astellas Pharma
Development Scientist Biopharma
Advanced degree in scientific or clinical disciplineSolid experience in industry environmentExpertise in clinical drug development lifecycle~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAThis role involves leading the design, execution, and analysis of high-quality clinical studies to advance innovative therapies
Warsaw, PolandPraca na miejscuWymagane doświadczenieWynik dopasowania do stanowiskaUtwórz profil22 dni temuBristol Myers Squibb
Senior Manager, Global Clinical Science - Cardiovascular
Degree in life sciences (md, phd, pharm d)Basic knowledge of gcp/ich regulationsIntermediate medical writing skillsZł328,440 - zł397,992 py
The role involves designing and executing clinical trial activities while collaborating with cross-functional teams to conduct cardiovascular studies
Warsaw, Poland50% onsiteFull timeWymagane doświadczenieWynik dopasowania do stanowiskaUtwórz profil22 dni temuBristol Myers Squibb
Senior Manager, Global Clinical Science - Cardiovascular
Degree in life sciences (md, phd, pharm d, ms, rn)Basic knowledge of gcp/ich and drug development processIntermediate medical writing skills and terminologyZł328,440 - zł397,992 py
The role involves designing and executing clinical trial activities while collaborating with external partners like Key Opinion Leaders
Warsaw, Poland50% onsiteFull timeWymagane doświadczenieWynik dopasowania do stanowiskaUtwórz profil22 dni temuBristol Myers Squibb
Senior Manager, Global Clinical Science - Cardiovascular
Degree in life sciences (md, phd, pharm d, ms, rn)Basic knowledge of gcp/ich and drug development processIntermediate medical writing skills and terminologyZł328,440 - zł397,992 py
The role involves designing and executing clinical trial activities while collaborating with external partners like Key Opinion Leaders
Warsaw, Poland50% onsiteFull timeWymagane doświadczenieWynik dopasowania do stanowiskaUtwórz profil22 dni temuAbbVie
Pipeline Medical Science Liaison
Fluent in polish and englishAdvanced degree in health sciences1-2 years medical affairs experience~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAThe Pipeline Medical Science Liaison serves as a scientific expert dedicated to facilitating dialogue and supporting clinical research objectives across Poland
Warsaw, PolandRemoteFull time+2 lata doświadczeniaWynik dopasowania do stanowiskaUtwórz profil30 dni temuaerzteforum.info
Specialist, Global Clinical Solutions, Ecoa, Uat
Bachelor's degree or equivalent educationProven organizational and analytical skillsComputer proficiency and english fluency~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAThe role supports the delivery of electronic Clinical Outcome Assessment (eCOA) and related technologies for AstraZeneca's clinical development programs
Warsaw, PolandHybrydowaFull timeWymagane doświadczenieWynik dopasowania do stanowiskaUtwórz profil31 dni temuParexel
Senior Clinical Research Associate - Poland (warsaw/ Lodz/ Trojmiasto/bydgoszcz/ Cracow/katowice)- Fsp
Extensive experience in site managementMinimum 2 years independent monitoringKnowledge of clinical trial methodologyPln 230,000 to 270,000 py
You will be dedicated to a single client and responsible for all site management activities in assigned oncology studies
Warsaw, PolandFully remoteFull time+2 lata doświadczeniaWynik dopasowania do stanowiskaUtwórz profil31 dni temuBristol Myers Squibb
Global Trial Lead
Lead global clinical trials from start-up to close-outMinimum 4 years experience in clinical operationsManage project plans, budgets, and vendor relationshipsZł271.580 - zł329.085
This role involves leading cross-functional teams and vendors to deliver critical clinical trials on time, within budget, and in full compliance
Warsaw, Poland50% onsiteFull time+4y experienceWynik dopasowania do stanowiskaUtwórz profil32 dni temuBristol Myers Squibb
Principal Global Trial Associate
4-6 years clinical research experienceKnowledge of ich/gcp guidelinesExperience with ctms and etmf systemsZł239,890 - zł290,697 py
This role provides operational support for global interventional clinical trials from concept to final clinical study report
Warsaw, Poland50% onsiteFull time+6y experienceWynik dopasowania do stanowiskaUtwórz profil32 dni temuExact Sciences
Sr. Clinical Trial Specialist, Poland
Bachelor's degree in life sciences5 years clinical research experience1 year sponsor or cro experience173,000.00 zł - 284,000.00 zł py
The role involves overseeing day-to-day operations of assigned clinical studies to ensure successful execution of cancer research plans
Warsaw, PolandFull time+5 lat doświadczeniaWynik dopasowania do stanowiskaUtwórz profil46 dni temuExact Sciences
Sr. Clinical Trial Specialist, Poland
Bachelor's degree in life sciences5 years clinical research experience1 year sponsor or cro experience173,000.00 zł - 284,000.00 zł py
The role involves overseeing day-to-day operations of assigned clinical studies to ensure successful execution of cancer research plans
Warsaw, PolandNot specified; likely hybrid or onsite based on the nature of the role.Full time+5 lat doświadczeniaWynik dopasowania do stanowiskaUtwórz profil58 dni temuExact Sciences Corporation
Sr. Clinical Trial Specialist, Poland
Bachelor's degree in life sciences5 years clinical research experience1 year sponsor or cro experience173,000.00 zł - 284,000.00 zł py
The Sr. Clinical Trial Specialist will oversee day-to-day operations of assigned clinical studies to ensure successful execution of company research plans
Warsaw, PolandNot specified (assumed to be hybrid or onsite based on typical clinical roles).Full time+5 lat doświadczeniaWynik dopasowania do stanowiskaUtwórz profil58 dni temuBristol Myers Squibb
Senior Manager, Global Clincal Science - Cardiovascular
Design and execution of clinical trialsKnowledge of gcp/ich guidelinesProtocol and icf document developmentZł328,440 - zł397,992 py
The role involves designing and executing clinical trial activities while collaborating closely with cross-functional teams to conduct cardiovascular studies
Warsaw, PolandFull timeWymagane doświadczenieWynik dopasowania do stanowiskaUtwórz profil58 dni temuJohnson & Johnson
Associate Site Manager
0-2 years clinical trial monitoring experienceGood clinical practice (gcp) complianceSite initiation and close-out activities~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAThis role serves as the primary contact point between the Sponsor and the Investigational Site to ensure inspection readiness
Warsaw, Masovian, PolandFully remoteFull time+2 lata doświadczeniaWynik dopasowania do stanowiskaUtwórz profil67 dni temuICON
Sr. Clinical Research Associate
Clinical trial site monitoringGcp standards adherenceData integrity and participant safety~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAAs a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
Warsaw, PolandFull timeWynik dopasowania do stanowiskaUtwórz profil79 dni temuICON
Clinical Research Associate 1
Overseeing and coordinating clinical trialsEnsuring compliance with regulationsCollecting and analyzing critical data~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development
Warsaw, PolandFull timeWynik dopasowania do stanowiskaUtwórz profil79 dni temuICON Clinical Research, LP
Sr. Clinical Research Associate
Overseeing and managing clinical trial activitiesEnsure data integrity, participant safetyMonitoring clinical trial sites~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAAs a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
Warsaw, PolandFull timeWynik dopasowania do stanowiskaUtwórz profil80 dni temuICON Clinical Research, LP
Clinical Research Associate 1
Overseeing and coordinating clinical trialsEnsuring compliance with regulationsCollecting and analyzing critical data~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAICON plc is a world-leading healthcare intelligence and clinical research organization focused on shaping the future of clinical development
Warsaw, PolandFull timeWynik dopasowania do stanowiskaUtwórz profil80 dni temuICON Clinical Research, LP
Clinical Trial Associate
Clinical trial documentationRegulatory requirements complianceCross-functional team communication~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAAs a Clinical Trial Associate at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innvative treatments and therapies
Warsaw, PolandFull timeWynik dopasowania do stanowiskaUtwórz profil80 dni temuICON Clinical Research, LP
Clinical Research Associate Ii/senior Cra
Conduct site visitsEnsure protocol complianceData integrity and patient safety~PLN 234,945 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAAs a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies
Warsaw, PolandFully remoteFull time+2 lata doświadczeniaWynik dopasowania do stanowiskaUtwórz profil80 dni temuICON Broadbean
Sr. Clinical Research Associate
Clinical trial site monitoringAdherence to study protocolsGcp standards compliance~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAAs a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
Warsaw, PolandFull timeWynik dopasowania do stanowiskaUtwórz profil80 dni temuICON Broadbean
Clinical Research Associate 1
Overseeing and coordinating clinical trialsEnsuring compliance with regulationsCollecting and analyzing critical data~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Clinical Research Associate to join their team
Warsaw, PolandFull timeWynik dopasowania do stanowiskaUtwórz profil80 dni temuICON plc
Sr. Clinical Research Associate
Overseeing and managing clinical trial activitiesEnsure data integrityParticipant safety~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAAs a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
Warsaw, PolandFull timeWynik dopasowania do stanowiskaUtwórz profil80 dni temuICON plc
Clinical Research Associate 1
Overseeing and coordinating clinical trialsEnsuring compliance with regulationsCollecting and analyzing critical data~PLN 230,000 – PLN 397,992 py
SZACOWANA WARTOŚĆ WORKOPIAICON plc is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence
Warsaw, PolandFull timeWynik dopasowania do stanowiskaUtwórz profil80 dni temuIQVIA
Experienced Clinical Research Associate, Site Management Poland
Perform site monitoring visitsTrack subject recruitment planEvaluate site quality and integrity132.800,00 zł - 280.000,00 zł
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements
Warsaw, PolandFull timeWynik dopasowania do stanowiskaUtwórz profil80 dni temu
SZACOWANA WARTOŚĆ WORKOPIA Wyświetlane, gdy pracodawca nie podaje wynagrodzenia. Jest to typowy zakres (percentyl 25–75) wynagrodzeń ujawnionych dla tej samej pozycji w tym samym mieście, dostosowany do poziomu doświadczenia i aktualizowany codziennie – szacunkowa wartość, a nie rzeczywista liczba podana przez pracodawcę.
