Research Study Coordinator Manager

Role Overview:The Clinical Research Associate will play a critical role in supporting the execution of clinical trials at study sites. This position requires excellent organizational, communication, and problem-solving skills, with a focus on ensuring high-quality data and compliance with regulations.Main Responsibilities:Site management and monitoring...

Job Description:Role OverviewThe Patient Recruitment and Engagement team is a specialized unit within our organization, focused on clinical study patient recruitment and retention. As a critical support function to this team, the Project Coordinator I will play a vital role in ensuring successful, timely, and quality delivery of projects.This position will...

We are seeking a highly skilled Study Management Coordinator to join our Data Management team at GlaxoSmithKline. As a key member of the team, you will be responsible for overseeing end-to-end study-related activities and ensuring the delivery of high-quality data management solutions.The ideal candidate will have experience in clinical data management...

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...

About the Job:The Global Study Manager is a key professional responsible for ensuring the successful delivery of clinical studies worldwide. As part of our global study team, you will play a crucial role in overseeing study execution, collaborating with internal and external stakeholders, and driving study progress.This role requires strong leadership and...

About the Role:The Global Study Manager will be responsible for supporting the delivery of clinical studies within Global Medicines Development (GMD) to time, cost, and quality.This role will involve working cross-functionally with internal and external partners to deliver delegated aspects of the clinical study in accordance with the Global Study Associate...

Job SummaryWe are seeking a highly experienced Centralized Monitoring Manager to join our team at PSI CRO.The successful candidate will have strong leadership skills, excellent communication abilities, and experience in clinical study management.Key responsibilities include:Leading and facilitating initial and ongoing study Risk Management...

Job Summary:The Global Study Manager role is a critical position within our organization, supporting the delivery of clinical studies worldwide. As a member of an extended global study team, you will work closely with internal and external partners to ensure timely, cost-effective, and high-quality study execution.This leadership role involves...

Job Role:The Clinical Trial Vendor Manager will be responsible for overseeing vendor performance, ensuring timely delivery of high-quality services, and driving process improvements to enhance vendor efficiency. This individual will collaborate with cross-functional teams to achieve business objectives and contribute to the overall success of our clients'...

Clinical Research Associate - IQVIA Biotech PolandIQVIA Biotech is hiring professionals to support the success of clinical trials.Contribute to improving patients' outcomes by joining IQVIA today.Job OverviewWe are looking for a skilled Clinical Research Associate to perform monitoring and site management work. The role involves ensuring that sites conduct...

Study Manager Position:We are looking for an experienced Study Manager to join our global study team. In this role, you will be responsible for managing clinical studies from start to finish, working closely with internal and external stakeholders to ensure successful study delivery.You will oversee study execution, prepare delegated study documents, and...

Clinical Research Associate - IQVIA Biotech PolandIQVIA Biotech seeks experienced professionals to manage clinical trials.Join us at IQVIA and make a difference in patients' lives.Job OverviewThe Clinical Research Associate will be responsible for performing monitoring and site management tasks to ensure compliance with study protocols, regulations, and...

About the Job:We are seeking a highly skilled and experienced Global Study Manager to join our team at TN Poland. The successful candidate will be responsible for managing clinical studies from initiation to closure, ensuring timely delivery, within budget and to the required quality standards.Main Responsibilities:To oversee the delivery of clinical studies...

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...

We are seeking a highly motivated Global Clinical Operations Coordinator to join our team at TN Poland. As a key contributor to our clinical operations department, you will be responsible for coordinating and supporting logistics for clinical trials.Responsibilities:Coordinate study/site supply management during pre-activation and subsequent course of the...

About the Role:We are looking for a Research Manager or Senior Research Manager to strengthen our team in Germany.As a Research Manager, you will support globally renowned clients across different industries with research design and delivery of insights. Our research practice supports clients with insights across FMCG, healthcare, automotive, technology,...

Role SummaryNMS Market Research s.r.o. is looking for a talented Regional Development Manager to lead our business development efforts in the Polish market research sector.Main Responsibilities

Job TitleClinical Research Associate SMDescriptionThis is an exciting opportunity to join our team as a Clinical Research Associate. The successful candidate will be responsible for performing site monitoring visits, working with sites to adapt and track subject recruitment plans, administering protocol and related study training, and ensuring site documents...

Social network you want to login/join with:Clinical Study Builder (European Economic Area)At TN Poland, we are seeking a highly skilled Clinical Study Builder to join our team.This role is ideal for individuals who have a passion for medical research and enjoy working in a dynamic environment.The successful candidate will be responsible for designing and...

Rho, Inc. is a leading Contract Research Organization (CRO) dedicated to providing exceptional service and expertise to pharmaceutical companies worldwide. Our mission is to improve human health by advancing medical research and development.About the JobWe are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our team. As a...