Clinical Research Associate

Experienced Clinical Research Associate (CRA)August Research, an Everest Clinical Research company, is looking for an experienced Clinical Research Associate (CRA) to join our team in Warsaw, Poland.This is a full-time CRA position for a candidate with at least one year of monitoring experience. Job responsibilities will include site identification and site...

ICON Clinical Research Clinical Research Coordinator (Przemysl, Poland) in Warsaw, PolandClinical Research Coordinator - Przemysl, Poland - FTICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to...

Job SummaryThe Clinical Research Associate will be responsible for managing clinical trials, including conducting site initiation visits, monitoring site performance, and ensuring compliance with study protocols. This role requires strong communication and interpersonal skills, as well as the ability to work effectively in a fast-paced...

About the TeamWe are a dynamic team at TN Poland, working together to deliver high-quality clinical research services to our clients. Our team is passionate about making a difference in people's lives through the advancement of medical knowledge and treatment options.We are seeking an experienced Associate Clinical Research Manager to join our team and lead...

Job DescriptionWe are seeking a skilled Clinical Research Associate to join our team in Warsaw, Poland. As a Senior Research Professional, you will play a critical role in the success of our clinical trials.Your responsibilities will include:Performing site selection, initiation, monitoring and close-out visitsSupporting the development of a subject...

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 CRFs;Collects, reviews, and monitors required regulatory...

Job SummaryCare Access Research is seeking a highly skilled and experienced Clinical Research Site Manager to oversee the day-to-day activities at our research site in Warsaw, Poland. As a key member of our team, you will be responsible for ensuring the successful execution of clinical trials, maintaining adherence to local regulations and Care Access SOPs,...

About the RoleCare Access Research is seeking a highly skilled and experienced Clinical Research Site Manager to oversee the day-to-day activities at our site in Warsaw, Poland. As a key member of our team, you will be responsible for ensuring the successful delivery of clinical trials while maintaining adherence to local regulations and CARE SOPs.Key...

As a Clinical Research Coordinator at ICON plc, you will play a critical role in supporting Investigator Site staff in conducting clinical research studies. This involves assisting in study-related activities at the site level, ensuring compliance with protocols, Standard Operational Procedures (SOPs), and international and local clinical trial...

About the RoleThe Site Manager will be responsible for leading the site's operations, managing personnel, and developing strategies to meet enrollment goals. This includes working closely with the Country Manager to ensure timely responses to feasibility questionnaires and scheduling of Site Evaluation Visits.Key Requirements:Master's degree required.2+...

Clinical Research Associate - Client DedicatedIn this role, you will provide critical support to our clinical research associates, ensuring the successful execution of clinical trials. Your expertise will help identify potential investigators, develop and distribute initial protocol packets, and ensure that all necessary documents are properly logged and...

Social network you want to login/join with:Clinical Research Associate, CDC - Talent Pipeline, WarsawClient:Location: Warsaw, PolandJob Category: OtherEU work permit required: YesJob Reference: 11b15dba9fecJob Views: 38Posted: 23.01.2025Expiry Date: 09.03.2025Job Description:The positionAs Clinical Research Associate your role is to verify the accuracy and...

Company OverviewThermo Fisher Scientific is a global leader in the life sciences industry, providing innovative solutions for customers in the pharmaceutical, biotechnology, and academic research markets.We are committed to advancing scientific research and improving human health through our cutting-edge technologies and services. Job DescriptionThe Remote...

Company DescriptionWhy 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 goals and culture that unites us across...

About the Role:Clinical Research Associates are needed to ensure that sites conducting clinical trials are performing as required by the study protocol, regulations, and sponsor requirements.Key Responsibilities:Perform site selection, initiation, monitoring, and close-out visitsSupport subject recruitment plan developmentMaintain regular lines of...

Brief DescriptionThe Clinical Programmer will be responsible for the provision of data review and trial management deliverables across all compounds and trials for which these are required, and for all functional groups that require those deliverables.Essential Functions/ResponsibilitiesProgram simple to complex data review listings, exception reports,...

About the RoleWe are looking for a skilled Clinical Research Coordinator to join our team in Warsaw, Poland. As a Clinical Research Coordinator, you will be responsible for conducting clinical remote monitoring visits and other clinical research activities in accordance with Study Protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (ICH...

Social network you want to login/join with:Experienced Clinical Research Associate SM, WarsawClient:IQVIALocation:Warsaw, PolandJob Category:OtherEU work permit required:YesJob Reference:23dbfc09693dJob Views:2Posted:17.03.2025Expiry Date:01.05.2025Job Description:Our team is growing, join us on our mission to drive healthcare forwardWhat We Offer / USPsThe...

Social network you want to login/join with:As a CRA at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.You will conduct onsite monitoring visits and be responsible for site...

IQVIA Biotech is hiring Clinical Research AssociatesJoin IQVIA today and make an impact on patients' outcomeJob OverviewPerform 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 guidelines, and sponsor...