What is expected to be done? Conducts feasibility studies and site qualification visits; Develops and ensures a strong site relationship through all phases of the trial; Gains in-depth understanding of the study protocol and related procedures; Prepares study documentation eg draft protocols, draft
If you want to: Join a multi-award-winning leading biopharmaceutical company Be part of growing team of Clinical Research Associates Use new technology and smart monitoring tools Have flexibility of work and good work-life balance Apply today In this role, you will be accountable for performance and...
10 000 - 15 000 PLN brutto miesięcznieAre you interested in collaborating with leading pharma companies to help patients all around the world? When you join IQVIA as a sponsor-dedicated Senior CRA in Poland, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with...
Join us in redefining what it means to work for a CRO. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges. At Rho, we’re committed to you just as
Are you a dedicated clinical trial professional with solid site management experience? Are you highly motivated by being able to make a difference to improving patients’ lives? If yes, keep reading – this role might be just for you! The position As Clinical Research Associate your role is to ve...
Overview Join us in redefining what it means to work for a CRO. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges. At Rho, we’re committed to you...
Why PSI? Because we are not a huge corporation and people still matter here. Our managers and employees have autonomy in making decisions and creating an engaging work environment. We provide the operational freedom to make nuanced country and department-specific adjustments, adhering to our common...
Poszukujemy (S)CRA z min. 2-letnim doświadczeniem dla firmy CRO o ustabilizowanej pozycji na międzynarodowym rynku, otwierającej biuro w Warszawie. Jest to idealna okazja dla osoby pracującej w dużej firmie, aby zdobyć doświadczenie w składaniu wniosków, negocjacji kontraktów, jak również zarządza...
Senior CRA Job Scope: The Senior CRA will be assigned clinical monitoring activities in a single country or in several countries ensuring quality service and appropriate clinical study conduct. The Senior CRA shall guarantee the adequacy, the reliability and quality of the data collected from site...
Clinical Research Associate, Single Sponsor dedicated in POLAND page is loaded Clinical Research Associate, Single Sponsor dedicated in POLAND Apply locations Warsaw, Poland Warsaw, Poland time type Full time posted on Posted Yesterday job requisition id R1416180 IQVIA is hiring Clinical Researc...