Study Management Specialist

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...

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...

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...

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 Operations Lead is responsible for ensuring the smooth execution of clinical studies globally. This includes overseeing study documents, interacting with internal and external functions, and contributing to meeting planning and conduct.To be successful in this role, one must have excellent stakeholder management and project...

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...

Global Study DirectorWe are seeking an experienced Global Study Director to lead our global study initiatives. As a seasoned professional, you will be responsible for overseeing global studies, developing research strategies, and collaborating with clients.ResponsibilitiesDevelop and implement research strategies to meet client needs.Oversee global studies,...

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 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...

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...

About the JobThis is an exciting opportunity to become a part of our esteemed organization as a Management Advisory Specialist. You will be responsible for providing expert advice to clients on strategic planning, risk management, and financial optimization.The ideal candidate will have strong analytical skills, excellent communication abilities, and a...

Job OverviewWe are seeking a highly skilled Associate Director to lead our Evidence Project Management team in Warsaw.About the RoleThe successful candidate will be responsible for coordinating and managing timely contributions of core/extended members, interfacing with key stakeholders, and reviewing protocol drafts.Key ResponsibilitiesCo-ordinate/manage...

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 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...

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 Research OperationsWe're seeking a skilled Clinical Research Operations professional 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.Review regulatory documents for proper content.Liaise with monitors and investigative sites to resolve...

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 seeking a skilled Clinical Research Associate to support clinical trial operations.Make an impact at IQVIA and contribute to improving patient care.Job SummaryWe are looking for a detail-oriented Clinical Research Associate to perform monitoring and site management duties. This includes...

Management Solutions, SL is a leading international consulting firm delivering business, risk, financial, organisational, and process-related advisory services targeting both functional aspects and the implementation of related technologies.We are currently seeking recent graduates or final year students to join our team as Management Solutions experts. In...

Job DescriptionWe are seeking a highly skilled Procurement Specialist to join our team in Contract Management.As a key member of our Global Procurement department, you will play a vital role in supporting Third-Party Risk Management processes, including contract drafting and negotiations.You will work closely with our procurement and business partners to...