Trial Management Specialist

About the RoleWe are seeking an experienced Trial Operations Associate to join our team.In this role, you will be responsible for supporting the management of clinical trials from start-up to close-out.You will work closely with investigators, site staff, and other stakeholders to ensure that trials are managed effectively and efficiently.The ideal candidate...

Role Summary:We are seeking a skilled Clinical Trial Vendor Manager to join our team. This individual will be responsible for managing vendor relationships, coordinating study start-up activities, and monitoring vendor performance to ensure timely delivery of high-quality services.Key Responsibilities:Develop and maintain strong relationships with vendors to...

Senior Clinical Trial Specialist RoleKey Responsibilities:Lead research efforts for new business opportunitiesSupport local country site outreach efforts for new business opportunities and awarded studiesAssess key study elements that impact investigator interest and patient enrollmentReview scientific literature, industry benchmarking, competition and...

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...

Clinical Trial OperationsAt TN Poland, we're committed to delivering high-quality clinical trial operations that meet the evolving needs of our clients.We're seeking a highly organized and detail-focused Clinical Trial Operations professional to join our team. As a Clinical Trial Coordinator, you will play a critical role in ensuring the successful delivery...

Clinical Data Manager RoleHays Poland invites applications from motivated professionals looking to take on a new challenge as a Clinical Data Manager.The ideal candidate will have extensive knowledge of clinical data management principles, methods, and regulations, coupled with hands-on experience in implementing data management plans and overseeing data...

Job DescriptionAs a Senior Clinical Trial Specialist at PSI CRO, you will become an integral part of our international team responsible for providing feasibility services, contributing to the development of our business, and ensuring smooth and predictable conduct of newly awarded trials. If you are passionate about the feasibility aspect of clinical trial...

About the RoleWe are looking for a highly motivated Senior Clinical Trial Specialist - EU to join our team at TN Poland. As a member of our international team, you will be responsible for providing feasibility services, contributing to business development, and ensuring the smooth conduct of newly awarded trials.The scope of responsibilities will...

Job SummaryThis is an exciting opportunity to join our team at IQVIA as a Trial Master File Manager. The successful candidate will be responsible for managing TMFs and other related documents, ensuring compliance with applicable SOPs, processes, and study-specific requirements.Main AccountabilitiesManage TMFs and other related documents from creation through...

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...

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 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...

About the RoleWe are currently hiring a Freelance Clinical Project Manager to work remotely on a freelance basis, managing international Phase I-IV clinical trials.The successful candidate will have excellent leadership and organizational skills, with a proven track record of delivering projects on time and within budget.Main ResponsibilitiesManage...

We are seeking a skilled Drug Development Specialist to join our team at TN Poland. As an Associate Project Director, you will be responsible for overseeing and managing all aspects of clinical trials from start up through to final delivery.This role plays a pivotal part in ensuring the successful execution of trials, from initial planning through to...

Job OverviewClinical trials are a crucial part of bringing new drugs to the market faster, and at IQVIA Argentina, we're looking for a skilled Tactical and Operational Scientific Co-Ordinator to join our team. As a key member of our clinical trial delivery team, you'll work closely with clinical teams to improve patient outcomes.Essential...

Clinical Trial Manager II, Dermatology & RheumatologyJob Summary:The Clinical Trial Manager II (CTM II) is responsible for the operational management and oversight of clinical investigative sites as well as clinical monitoring deliverables of clinical trials.Responsibilities:Ensures timely quality deliverables and in accordance with applicable standard...

We are recruiting a highly skilled Clinical Trial Coordinator to join our team in Warsaw or Madrid.Role OverviewThe successful candidate will be responsible for developing, negotiating, and finalizing site agreements and budgets for medical device clinical trials across various therapeutic areas. They will collaborate with internal stakeholders and external...

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...

Transforming lives through clinical research is at the core of our mission at Thermo Fisher Scientific. As a leading global contract research organization, we are dedicated to improving health outcomes that people and communities depend on. Our purpose is to help customers deliver life-changing therapies, and our strategy is to bend the cost and time curve...

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...