Clinical Trial Support Coordinator

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...

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...

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...

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...

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...

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...

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...

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...

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...

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 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...

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...

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...

Job DescriptionWe are looking for a Clinical Trial Finance Professional to join our team in Poland.The successful candidate will be responsible for managing project finances, collaborating with project teams, clients, and internal departments to ensure financial performance and high-quality clinical research project management services.This role requires...

Job OverviewWe are seeking a highly motivated and detail-oriented Clinical Trial Assistant to join our team at ICON Strategic Solutions. As a key member of our clinical operations team, you will be responsible for providing support to Site Managers (CRA) by distributing and tracking investigator feasibility questionnaires, as well as summarizing results.In...

About UsRho, Inc. is a full-service Contract Research Organization (CRO) based in North America.We offer a comprehensive benefits package for all benefit-eligible employees and encourage a work-life balance that allows employees to bring their best selves to work.Job Title: Freelance Clinical Project ManagerMain ResponsibilitiesManage international clinical...

Role SummaryThis is a full-time position as a Clinical Trials Coordinator, requiring a College/University degree in Life Sciences or an equivalent combination of education, training, and experience. The ideal candidate should have minimum 2 years of experience in independent on-site monitoring in Poland and full working proficiency in Polish, English, and MS...

Job DescriptionWe are seeking a highly motivated and experienced individual to join our team as an Clinical Operations Coordinator. In this role, you will be responsible for evaluating the performance of a team to ensure compliance with expectations. You will collaborate with internal and external stakeholders to create and deliver training content to...

OverviewJoin us in redefining what it means to work for a CRO. Dokumeds has become part of Rho, an award-winning, full-service CRO based in North America. As one company, we will deliver global full-service clinical development services and unmatched customer support – worldwide. Working at Rho, you'll be joining a team who take healthcare and clinical...