Research Study Coordinator

About the PositionWe are currently seeking a Regulatory Compliance Coordinator to join our team at Care Access Research. As a Regulatory Compliance Coordinator, you will be responsible for overseeing the accuracy and quality of data for research projects within designated research sites.ResponsibilitiesOverseeing the accuracy and quality of data for research...

About the Role:We are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our Clinical Operations team in Poland, Estonia, Lithuania, or Latvia. The successful candidate will have experience in Clinical Trials and possess excellent organizational, communication, and teamwork skills.Key Responsibilities:Preparation of ISFs...

OverviewRho is a global contract research organization (CRO) dedicated to healthcare and clinical research. We take a personalized approach to working with our clients, understanding their unique needs and challenges.We are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our team in Poland, Estonia, Lithuania, or Latvia. As a...

Global Study Manager - Biopharma (12 months fixed term contract/secondment), WarsawClient:Location: Warsaw, PolandJob Category: OtherEU work permit required: YesJob Reference: 25231bc49ec4Job Views: 25Posted: 23.01.2025Expiry Date: 09.03.2025Job Description:The Global Study Manager is a member of an extended global study team supporting the delivery of...

Job Summary:This Clinical Research Associate position is an excellent opportunity for individuals passionate about clinical research and patient outcomes. As a key member of our team, you will contribute to the success of clinical trials, working closely with study sites, sponsors, and internal stakeholders to ensure seamless project execution.Main...

Job OverviewCare Access is a pioneering organization that revolutionizes access to clinical trials for the benefit of patients everywhere. As a clinical research site director, you will be responsible for overseeing the day-to-day activities at our site under the direction of the Country Manager. Your primary objective will be to ensure delivery of...

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...

About the RoleWe are seeking a highly skilled Senior Research Analyst to join our team in Warsaw. As a key member of our European software research team, you will be responsible for conducting market research and analysis on enterprise applications.As a Senior Research Analyst, you will have the opportunity to work closely with our global counterparts and...

About this OpportunityWe are seeking a qualified Clinical Research Associate to join our team at IQVIA.The role involves:Performing site selection, initiation, monitoring and close-out visitsContributing to the development of a subject recruitment strategyDeveloping and implementing protocol and related study training plans for assigned sitesEnsuring the...

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...

OverviewJoin 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 you're committed to us. You'll have the opportunity to...

GfK Boutique Research OverviewAs the world's leading consumer intelligence company, we deliver unparalleled insights into consumer buying behavior and growth opportunities. Our mission is to empower businesses to make informed decisions and drive growth through our advanced analytics capabilities.We're proud to have brought together two industry leaders –...

You are a skilled project coordinator who thrives in a fast-paced environment. At Sonova, we offer exceptional career opportunities through market-leading brands from consumer to medical, products and services that keep pushing hearing care forward.As Senior Project Coordinator, you will directly report into the Director Global HR Program Management and...

IQVIA is hiring Clinical Research AssociatesJoin IQVIA today and make an impact on patients' outcomesJob 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 requirements.ResponsibilitiesPerforming...

We are seeking a Business Development Coordinator to join our EU Expansion team. As a key member of our team, you will be responsible for identifying and pursuing new business opportunities to drive growth and expansion of our marketplace in Poland and across Europe.Responsibilities:Identifying and pursuing new business opportunities to drive growth and...

About UsGfK Boutique Research is the world's leading consumer intelligence company, delivering unparalleled insights into consumer buying behavior and growth opportunities.We combine our industry-leading expertise with state-of-the-art platforms to provide comprehensive consumer insights. Our mission is to empower businesses to make informed decisions and...

Job Description:We are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our Clinical Operations team in Poland, Estonia, Lithuania, or Latvia. The successful candidate will have experience in Clinical Trials and possess excellent organizational, communication, and teamwork skills.Key Responsibilities:Preparation of ISFs...

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...

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...

About the RoleClinical Research Associates are needed to work with us at IQVIA.Key Responsibilities:Site selection, initiation, monitoring and close-out visitsSupporting subject recruitment planningDeveloping protocol and related study training plans for sitesEvaluating site practices and escalating quality issuesTracking regulatory submissions, case report...