Senior Clinical Trial Specialist

Are you an expert in graphic design looking to apply your skills in a fast-paced environment? Do you have a passion for creating visually appealing documents?We're seeking a highly skilled Clinical Trial Document Specialist to join our team at PSI CRO. As a specialist, you'll be responsible for designing and developing clinical trial documents that meet...

Job Description: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...

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...

The Clinical Trial Support Coordinator role at TN Poland involves providing support to clinical trial teams through troubleshooting, problem identification, solution identification and resolution.Key ResponsibilitiesProvide technical support to clinical trial teams.Collaborate with cross-functional teams to resolve issues.Analyze data to identify trends and...

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...

TN Poland is seeking a detail-oriented and organized individual to fill the role of Associate Site Manager.Responsibilities:The Associate Site Manager will be responsible for ensuring site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases.This role also involves contributing to site...

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...

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 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...

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...

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...

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...

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...

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...

About the RoleWe are seeking a highly skilled Clinical Documentation Specialist to join our team at IQVIA. As a key member of our organization, you will be responsible for ensuring the efficient and effective management of Trial Master Files (TMFs) and other related documents.Main ResponsibilitiesDrive TMF quality at the trial level by acting as a single...

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 (Investigator Site...

Job SummaryThis position involves working as a senior-level safety scientist on various clinical trials, ensuring that all aspects of trial operations meet the highest standards. The ideal candidate will have extensive knowledge of clinical trials, data review tools, and regulatory guidelines, as well as excellent analytical and communication skills. This...

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...

Job DescriptionAt TN Poland, we are seeking a highly skilled Clinical Research Professional to join our international team. As a Senior Clinical Trial Specialist, you will play a crucial role in providing feasibility services, contributing to business development, and ensuring the smooth conduct of newly awarded trials.This is an excellent opportunity for...

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...