Praca Clinical Site Manager

A leading global clinical research organization is seeking a Site Contract Manager based in Warsaw, Poland. The successful candidate will develop global contracting strategies and support clinical trials by providing specialized legal, operational, and financial contracting support. The ideal candidate should have at least 5 years of relevant experience and strong negotiation skills, alongside a...

A leading global clinical research firm in Poland seeks a Contracts Specialist to develop and implement contracting strategies for clinical studies. Responsibilities include negotiating contracts, ensuring compliance with regulations, and providing legal support. Candidates should have a Bachelor's degree and at least 5 years of relevant experience. The role requires strong negotiation,...

A leading clinical research organization in Poland seeks a Site Selection Lead to provide functional leadership for the site selection process. This role includes acting as the primary contact for studies, ensuring the delivery of milestones, and managing site profiles tailored for various protocols. The ideal candidate will have a Bachelor's Degree and 3-6 years of experience in a clinical...

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...

A global clinical study support organization in Poznań is seeking a Site Coordinator. You will be responsible for facilitating communications between the Sponsor and the study site, ensuring enrollment goals are met, and maintaining compliance with clinical trial protocols. Candidates should have a Life Science degree and at least 2 years of site coordination experience. The position offers a...

A leading biopharmaceutical solutions organization in Warsaw seeks a qualified Clinical Research Associate to perform site management and clinical monitoring activities. This role requires a Bachelor's degree or equivalent in a related field, strong communication skills, and knowledge of Good Clinical Practice. The ideal candidate will support regulatory compliance and ensure proper conduct of...

A global pharmaceutical company is seeking a Clinical Payments Supervisor to oversee daily operational activities within the clinical team. This role involves managing contracts and payments processes and leading a team, requiring over 8 years of relevant experience in clinical budgets and strong analytical skills. The ideal candidate should possess leadership and project management experience...

Overview Global Monitoring and Site Engagement (GMASE) Global Process Owner (GPO) — Clinical Operations Join to apply for the Global Monitoring and Site Engagement (GMASE) Global Process Owner (GPO) — Clinical Operations role at GSK. Position Summary The GMASE Global Process Owner (GPO) is a senior clinical operations leader who designs, governs and continuously improves clinical operational...

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 leading biopharmaceutical solutions organization in Warsaw is seeking a Clinical Research Associate to ensure compliance and integrity of clinical research studies. The ideal candidate will have a Bachelor’s degree, strong communication skills, and the ability to manage significant travel. Responsibilities include site management, data verification, and supporting clinical trials with...

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 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 biopharmaceutical solutions organization is seeking a Clinical Research Associate (CRA) to ensure the integrity of clinical trials. In this role, you will verify compliance with regulations and clinical protocols while conducting remote and on-site monitoring activities. Ideal candidates will have a relevant degree and knowledge of Good Clinical Practice guidelines. This full-time...

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 biopharmaceutical solutions organization is seeking a Clinical Research Associate to perform site management tasks, including qualification, initiation, monitoring, and close-out activities. The ideal candidate will have a Bachelor's degree or RN in a related field, with excellent communication and interpersonal skills. A good understanding of Good Clinical Practice and ICH Guidelines...

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 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 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 clinical research organization is seeking a Site Coordinator in Częstochowa, Poland. You will support trial sites by managing communications, ensuring timely responses to feasibility questions, and tracking patient enrollment. The ideal candidate holds a degree in Life Science and has experience in clinical trial coordination. This role offers the opportunity to work in a fast-paced environment...

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...