Study Management Lead

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...

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...

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...

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...

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...

We are looking for an experienced Clinical Data Specialist Lead to join our Data Management team at GlaxoSmithKline. As a key member of the team, you will be responsible for providing DM operational input into study design, protocol, and study planning.The ideal candidate will have experience in clinical data management processes, standards, and systems, as...

About the RoleThe Centralized Monitoring Manager will play a critical role in ensuring patient safety and data integrity through the implementation of risk-based monitoring approaches.The ideal candidate will have strong leadership skills, excellent communication abilities, and experience in clinical study management.Key Responsibilities:Lead and facilitate...

Site Name: WarsawPosted Date: Mar 13 2025We are looking for quickly learning, open minded and independent Data Lead who will be a part of the Data Management group within our constantly growing GSK R&D Polish Hub. This role is responsible for overseeing the end-to-end Data Management (DM) study related activities and is accountable for all Data Strategy &...

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...

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...

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...

Quality Assurance LeadWe are seeking a highly skilled Quality Assurance Lead to join our team at IQVIA. As a key member of our organization, you will be responsible for ensuring the quality and completeness of Trial Master Files (TMFs) and other related documents.Main ResponsibilitiesReview TMF quality early and during the study, using a targeted and...

Job DescriptionWe are seeking a highly skilled Clinical Trial Lead to join our team at PSI CRO. As a Central Monitoring Manager, you will be responsible for leading the implementation of risk-based monitoring approaches on clinical study and program levels.You will:Facilitate initial and ongoing study Risk Management activities.Participate in the selection...

Data Management PositionWe are seeking a highly skilled Data Management professional to join our team at Hays Poland.The successful candidate will be responsible for managing data across multiple clinical trials, ensuring seamless collaboration between cross-functional teams, and delivering high-quality data in accordance with regulatory requirements.Duties...

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'...

At TN Poland, we are looking for a skilled Clinical Research Associate Lead to join our team of professionals. As a key member of our clinical operations department, you will play a vital role in ensuring the success of our clinical trials.Job Description:Lead remote monitoring activities on assigned projects, working closely with our Remote CRA and On-Site...

About TN PolandTN Poland is a leading provider of clinical research services to the life sciences industry.Job DescriptionWe are seeking a highly skilled Clinical Research Associate to join our team. The successful candidate will be responsible for performing site monitoring visits, working with sites to adapt and track subject recruitment plans,...

Job DescriptionThis position is a key role in the development and maintenance of data quality standards. The successful candidate will lead the implementation and maintenance of internal data quality control programs, acceptance criteria for data from external sources, and perform related programming tasks.The ideal candidate will collaborate with the...

TN Poland is seeking a skilled Site Management Professional to join our team of professionals. As a key member of our clinical operations department, you will play a vital role in ensuring the success of our clinical trials.Job Overview:As a Site Management Professional, you will be responsible for performing site management tasks, including but not limited...

Job DescriptionWe are looking for a Document Management Strategist to join our team at IQVIA. As a key member of our organization, you will be responsible for defining and refining the document management strategy for Trial Master Files (TMFs) and other related documents.Main ResponsibilitiesDefine and refine the document management strategy for TMFs and...