Praca Clinical Study Manager

Clinical Trial Manager II – Study Manager in RWE (Poland, Bulgaria, UK, Romania, Spain) Join to apply for the Clinical Trial Manager II – Study Manager in RWE (Poland, Bulgaria, UK, Romania, Spain) – Sponsor‑dedicated role at Syneos Health . About Syneos Health Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We...

Clinical Trial Manager II - Study Manager in RWE (Poland, Bulgaria, UK, Romania, Spain) - Sponsor-dedicated Updated: December 22, 2025 Location: Warsaw, MZ, Poland Job ID: Description Clinical Trial Manager II - Study Manager in RWE (Poland, Bulgaria, UK, Romania, Spain) - Sponsor-dedicated Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to...

A leading clinical research organization in Warsaw is seeking a Site Management Associate (SMA I) to support operational study delivery. Key responsibilities include maintaining systems for study data quality, overseeing compliance, and coordinating study budgets. The ideal candidate will have a university degree, a minimum of two years of relevant experience, and strong knowledge of Good...

A global clinical study support organization is seeking a Site Coordinator to facilitate clinical trial activities at study sites in Puławy, Poland. The ideal candidate has a Life Science degree and at least 2 years of experience. Key responsibilities include communication with Sponsors, tracking patient enrollment, and supporting study audits. This position may require flexibility in working...

A leading pharmaceutical company is seeking a Global Study Manager to support clinical studies in their Cell Therapy division. The role involves cross-functional collaboration, preparation of study documents, and ensuring studies meet quality and regulatory standards. The ideal candidate has a Bachelor's degree in medical or biological sciences and at least 5 years of experience in clinical...

Clinical Trial Associate - US (Study Start-Up Support) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. What you will be doing - The SSU Clinical Study Administrator is responsible for...

A clinical research organization is seeking a Site Coordinator based in Poland to support clinical trial activities. This role involves acting as the main communication line between the Sponsor and the site, assisting in monitoring visits, and ensuring patient enrollments meet project timelines. Ideal candidates will have a Life Science degree and at least 2 years of experience as a site...

A leading clinical research organization based in Poland is seeking a Site Management Associate I to ensure operational study delivery. The role involves maintaining internal systems, supporting study coordination, and overseeing compliance with regulatory requirements. Ideal candidates will have a scientific degree, two years of relevant experience, and a deep understanding of clinical research...

A clinical trial support organization is seeking a Site Coordinator to assist with clinical trial activities, ensuring communication between sponsors and sites. The role requires a university degree in a relevant field and a minimum of 2 years of site coordinator experience. Responsibilities include managing patient enrollment, coordinating monitoring visits, and ensuring compliance with study...

A leading pharmaceutical company seeks a Clinical Research Lead in Poland. The role involves overseeing clinical studies, ensuring compliance with applicable regulations, and collaborating with internal stakeholders. Candidates should possess at least 5 years of experience in clinical research and a relevant Bachelor's degree. Strong communication and teamwork skills are essential. The position...

The Sr. Manager, Study Start-Up is responsible for overseeing and driving all global and regional activities related to clinical study start up, site feasibility, site selection, contract and budget negotiations, and site activation. This role ensures timely, high-quality, and compliant study start-up deliverables to support the successful execution of clinical trials across the organization’s...

A leading drug development services company is looking for a Global Study Manager to oversee clinical trial projects. This temporary position requires strong project management skills and at least 2 years of industry experience. The role involves managing client relations and ensuring successful study delivery while providing exceptional customer service. Candidates should have a relevant...

1 day ago Be among the first 25 applicants This range is provided by Alimentiv. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range Responsibilities Strategic Leadership - Develop and implement global and regional strategies for efficient study start-up operations - Define key performance indicators (KPIs) to monitor progress,...

Join to apply for the Global Study Manager (temporary role) role at Labcorp 4 days ago Be among the first 25 applicants Get ready to redefine what’s possible and discover your extraordinary potential . Here at Labcorp, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of...

In AstraZeneca's Cell Therapy division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying, and even curing some of the world's most complex diseases. We have the potential to grow our pipeline and positively impact the lives of patients around the world. We are committed to making a difference and have built our business around our passion for...

A clinical study services provider is seeking a Site Coordinator in Poznań, Poland. The role involves supporting clinical trial activities, ensuring effective communication between the sponsor and study site, and handling various administrative tasks related to patient enrollment and monitoring. A university degree in Life Science and at least 2 years of experience as a site coordinator are...

A leading clinical research organization is seeking a Study Start Up Associate II for a hybrid role based in Poland. The candidate should have a Bachelor’s Degree in Life Sciences and 2-4 years of experience in clinical study start-up activities. Responsibilities include supporting site partners and maintaining regulatory compliance. This organization offers competitive benefits, a focus on...

A leading Contract Research Organization is seeking a Study Startup Assistant in Warsaw, Poland. This role is a fixed-term contract for 12 months, offering the opportunity to gain experience in Clinical Trials. Responsibilities include providing administrative support for site activation, assisting in research and site identification, and maintaining essential tracking systems. Ideal candidates...

A leading clinical research organization in Warsaw seeks a Site Management Associate to assist in monitoring clinical trial sites. You will ensure compliance with protocols and support site management activities. Ideal candidates hold a Bachelor's degree in relevant fields and have strong organizational skills. Join us to impact clinical research positively in a collaborative environment that...

An established industry player is seeking a dedicated Site Coordinator to support clinical trials at research sites. This role is essential in ensuring effective communication between sponsors and clinical sites, tracking patient enrollment, and maintaining study documentation. The ideal candidate will thrive in a fast-paced environment and possess excellent problem-solving skills. Join a company...