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
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
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...
Are 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
Do you know why we are one of only three CROs to have received the Leadership Award for 11 consecutive years? Because we appreciate our team, whose dedication and commitment to excellence is reflected in this award, and we work with heart, keeping the patient at the center of everything we do. Joi...
Primary Location Poland Job ID: PO_WA_CRA-0822 Job Type: Full-Time JOB DESCRIPTION Your main responsibilities: Perform site visits and monitoring activities in accordance with protocol, SOPs, GCP/ICH; Participate in study site selection, including on-site and remote (by phone) pre-study site evaluat...
IQVIA is hiring Clinical Research Associates! Join IQVIA today and make an impact on patients’ outcome! Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and g...
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...
As a Clinical Research Associate (CRA) you are an essential part of the clinical operations team responsible for coordinating and overseeing the execution of studies and clinical trial according to the study protocol, ICH-GCP, applicable regulations, guidelines and sponsor requirements. Some of w...
Job Description - Senior Clinical Research Associate (Senior Site Manager) (2406182788W) Senior Clinical Research Associate (Senior Site Manager) - 2406182788W Description A Senior Clinical Research Associate (Senior Site Manager) serves as the primary contact point between the Sponsor and the Inves...