Clinical Trial Operations Coordinator

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...

At Rho, Inc., we are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our team. As a member of our organization, you will play a vital role in the success of our clinical trials.About UsRho, Inc. is a leading Contract Research Organization (CRO) dedicated to providing exceptional service and expertise to pharmaceutical companies...

We are seeking a highly skilled Clinical Operations Assistant to join our team at Parexel International. As a key member of the site management team, you will be responsible for supporting the efficient management of clinical trials.This may include tasks related to site payments, management of site supplies, trial master file, site activation, Clinical...

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...

Company Overview:IQVIA Argentina is a leading provider of healthcare insights, technology, and services.We are seeking an experienced Clinical Trial Operations Specialist to join our team.Job Description:The successful candidate will be responsible for coordinating the operational and strategic aspects for clinical trial submissions.Essential Functions:Lead...

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...

We are currently hiring a Freelance Regional Clinical Trial Coordinator to join our team This can be home-based in Poland, Estonia, Lithuania, or LatviaResponsibilitiesThe Freelance Regional Clinical Trial Coordinator will be responsible for supporting the preparation of Investigator Site Files, maintaining the Trial Master File, and ensuring timely...

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...

Rho, Inc. is a leading Contract Research Organization (CRO) dedicated to providing exceptional service and expertise to pharmaceutical companies worldwide. Our mission is to improve human health by advancing medical research and development.About the JobWe are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our team. As a...

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...

Job OverviewWe are seeking a highly skilled Clinical Country and Site Lead to join our team at Biogen. This role will be responsible for providing strategic direction and oversight for clinical trials in Poland.The ideal candidate will have extensive experience in managing clinical trial activities, including sponsor oversight activities in an outsourced...

**Job Summary:**We are seeking a highly motivated and organized Global Clinical Contracts Coordinator to join our team at TN Poland. This role involves coordinating the development and implementation of clinical trial contracts and agreements, working closely with cross-functional teams to ensure compliance with regulatory requirements and company...

We are seeking a highly motivated Global Clinical Operations Coordinator to join our team at TN Poland. As a key contributor to our clinical operations department, you will be responsible for coordinating and supporting logistics for clinical trials.Responsibilities:Coordinate study/site supply management during pre-activation and subsequent course of the...

RequirementsEducation BSN/BS/MS or BA required.Minimum of 1 year experience in clinical environment as CTA.Excellent written and oral communication skills.Knowledge of Microsoft Office applications especially Excel.Ability to collaborate and build strong partnerships/relationships with all functions involved in the trial.Fluent English.Why ICON?Our success...

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...

Clinical Trial SupportWe're seeking a highly organized and detail-focused Clinical Trial Coordinator 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.Performs PPD investigator file reviews and logging of outstanding issues in project related...

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...

Parexel International is seeking a skilled Clinical Operations Assistant to join our team. As a key member of the site management team, you will support the efficient management of clinical trials by completing administrative tasks on behalf of the assigned Project Clinical Team.This may include tasks related to site payments, management of site supplies,...

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...