Praca Clinical Study Coordinator

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...

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...

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 clinical research organization is seeking a detail-oriented Central Study Coordinator for a part-time role based in Ostrava, Czech Republic. The ideal candidate will have a Bachelor's degree in Life Sciences or a related field, along with strong communication and organizational skills. Responsibilities include supporting clinical study operations, maintaining documentation, and ensuring...

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...

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 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...

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 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...

Part-Time | Up to 32 hours/week (flexible based on workload and patient recruitment) Start Date: As soon as available What You’ll Do - Prepare and organize study visits - Schedule patient appointments and coordinate reminders - Handle general administrative tasks and order lab kits - Support audit and inspection preparation and activities Requirements - Previous experience as a Study...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career...

Position: Freelancer- Central Study Coordinator Location: Ostrava, Czech Republic (On-site) Employment Type: Part-time – 6 hours per week, Wednesday (Freelancer Contract) Industry: Clinical Research / Life Sciences About the Role We are seeking a detail-oriented and proactive Central Study Coordinator to support the planning, execution, and oversight of clinical research studies. This...

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 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 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 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...

A global clinical services organization in Warsaw is seeking a Site Coordinator to support clinical trial activities. The chosen candidate will facilitate communication between sponsors and sites and ensure compliance with ICH-GCP standards. Ideal applicants should have a degree in Life Sciences and a minimum of 2 years of experience as a site coordinator. This role demands strong problem-solving...

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...

Company Description Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. Job Description Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within Study...