Clinical Study Specialist

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 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 OverviewAt TN Poland, we are seeking a highly skilled Clinical Operations Specialist to join our team. As a Centralized Monitor, you will play a critical role in the execution of clinical studies from initiation through closeout.Your primary responsibility will be to manage assigned sites and perform subject level data review independently or as part of...

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...

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...

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...

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...

Key Responsibilities:The Tactical and Operational Scientific Co-Ordinator will play a vital role in the successful delivery of clinical trials at IQVIA Argentina. Key responsibilities include:Leading bid defense presentations and managing smaller, less complex regional studies.Developing integrated study management plans with core project teams and...

Job DescriptionClinical Trial Safety Scientist:  Key Responsibilities  Ensure consistent processes and efficient review of critical clinical/safety data.Review patient-level clinical/safety data on an ongoing basis to ensure medical accuracy and completeness, coding consistency, and generate applicable queries as needed for appropriate medical assessment...

Your RoleAs a Director, Medical Review Scientist, you will be responsible for performing medical review activities across multiple oncology studies with a wide range of therapeutic modalities and tumor types.Key ResponsibilitiesDevelops a Medical Review Plan (MRP) for the study, which details the scope of the medical review and appropriate timelines s/he...

Clinical Research Coordination SpecialistICON plc is a leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development. We are seeking a skilled Clinical Research Coordination Specialist to join our team.As a member of our team, you will be responsible for facilitating project team and client...

Clinical Research SpecialistWe're seeking a skilled Clinical Research Specialist to join our team at TN Poland.In this role, you will be responsible for coordinating project administration tasks and providing technical support to project teams.Coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.Reviews...

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...

About the Role:The Global Study Manager will be responsible for managing clinical studies from initiation to closure, ensuring timely delivery, within budget and to the required quality standards.This role will involve working cross-functionally with internal and external partners to deliver delegated aspects of the clinical study in accordance with the...

Clinical Data ManagerAs a Clinical Data Manager at Hays Poland, you will be responsible for leading the planning and execution of data management methodologies for assigned clinical studies.You will collaborate with study teams to implement data management strategies and practices that ensure high-quality data delivery.Key responsibilities include designing...

IQVIA LLC is dedicated to helping patients access safe and effective medication through innovative clinical research services.Job DescriptionThe Sr Site Activation Specialist will serve as a liaison between investigative sites and IQVIA LLC, ensuring seamless execution of study activities.Communicate effectively with investigative sites and internal...

Clinical Study Manager Opportunity:We are seeking an experienced Clinical Study Manager to join our global study team. As a key professional in this role, you will be responsible for ensuring the successful delivery of clinical studies worldwide. This position requires strong leadership and communication skills, as well as the ability to navigate complex...