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
Learn more about our EEO & Accommodations request here.
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
Learn more about our EEO & Accommodations request here.
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