We are looking for an experienced CRA to join our sponsor-dedicated team in Poznań. This role offers the opportunity to work exclusively with one global sponsor providing strong study continuity deep therapeutic exposure and long-term career development.
Key Responsibilities: Conduct site monitoring visits (initiation routine and close-out) Ensure compliance with protocols SOPs and applicable regulations Perform source data verification and maintain high data quality standards Track and follow up on SAEs ensuring patient safety oversight Prepare accurate monitoring and trip reports Support feasibility activities site selection and investigator engagement Collaborate closely with sponsors investigators and internal teams Contribute to training and mentoring of junior team members
Requirements: 1.5 years of independent monitoring experience in Pharma/CRO Experience in interventional clinical studies Strong knowledge of SAE reporting Degree in Life Sciences Nursing or related field Fluency in English and Polish Oncology experience is a plus (or willingness to work in oncology studies)
What we offer: Dedicated role with one global sponsor Exposure to complex international clinical trials Clear career progression opportunities Supportive and collaborative team environment
Location: Poznań PolandWe are looking for an experienced CRA to join our sponsor-dedicated team in Poznań. This role offers the opportunity to work exclusively with one global sponsor providing strong study continuity deep therapeutic exposure and long-term career development. Key Responsibilities:...
Location: Poznań Poland
We are looking for an experienced CRA to join our sponsor-dedicated team in Poznań. This role offers the opportunity to work exclusively with one global sponsor providing strong study continuity deep therapeutic exposure and long-term career development.
Key Responsibilities: Conduct site monitoring visits (initiation routine and close-out) Ensure compliance with protocols SOPs and applicable regulations Perform source data verification and maintain high data quality standards Track and follow up on SAEs ensuring patient safety oversight Prepare accurate monitoring and trip reports Support feasibility activities site selection and investigator engagement Collaborate closely with sponsors investigators and internal teams Contribute to training and mentoring of junior team members
Requirements: 1.5 years of independent monitoring experience in Pharma/CRO Experience in interventional clinical studies Strong knowledge of SAE reporting Degree in Life Sciences Nursing or related field Fluency in English and Polish Oncology experience is a plus (or willingness to work in oncology studies)
What we offer: Dedicated role with one global sponsor Exposure to complex international clinical trials Clear career progression opportunities Supportive and collaborative team environment