Senior Clinical Study Coordinator

We are seeking a highly skilled Study Management Coordinator to join our Data Management team at GlaxoSmithKline. As a key member of the team, you will be responsible for overseeing end-to-end study-related activities and ensuring the delivery of high-quality data management solutions.The ideal candidate will have experience in clinical data management...

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...

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...

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...

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 Overview:The Clinical Research Associate will play a critical role in supporting the execution of clinical trials at study sites. This position requires excellent organizational, communication, and problem-solving skills, with a focus on ensuring high-quality data and compliance with regulations.Main Responsibilities:Site management and monitoring...

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'...

About the Role: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...

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...

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...

Social network you want to login/join with:Clinical Study Builder (European Economic Area)At TN Poland, we are seeking a highly skilled Clinical Study Builder to join our team.This role is ideal for individuals who have a passion for medical research and enjoy working in a dynamic environment.The successful candidate will be responsible for designing and...

Senior Clinical ProgrammerLocation: home-based in Eastern EU (Poland, Hungary, Serbia)Why IQVIAData Sciences Staffing Solutions, DSSS or DS3, is a unit within IQVIA that provides our sponsors with fully dedicated resources through a Functional Service Provider (FSP) partnership. This means you get all the benefits of working for an industry leading CRO while...

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...

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...

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...

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...

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...

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...

Career Advancement OpportunitiesThis role offers an exciting opportunity to work with a dynamic team and contribute to the success of our clients.The successful candidate will have a strong understanding of clinical data management and statistical programming processes and standards.Key Responsibilities:Lead the implementation and maintenance of internal...