CRA II

We are currently recruiting for our multisponsor team in Central or Southern Poland and are looking to hire a permanent, full-time CRA II.

Our positions offer excellent exposure to a range of disease areas, and a real opportunity for career progression and promotion in time.

• →Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned
• →Responsible for all aspects of site management as prescribed in the project plan
• →Ensure the study staff who will conduct the protocol have received the proper training, materials and instructions to safely enter patients into the study
• →Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
• →Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review
• →Monitor data for missing or implausible data
• →Ensure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines
• →Ensure audit readiness at the site level
• →Prepare accurate and timely trip reports
• →Participate in and follow up on Quality Control Visits (QC) when requested
• →Might be requested to work in a client facing environment
• →Track and follow up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAE
• →Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
• →Assist with training, of new employees, e.g. co-monitoring
• →Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned, when requested

We are searching for a university graduate with a life science degree or nursing background who relishes working in a fast paced environment, on complex and demanding protocols. 

If you are someone who is eager to constantly develop and improve while working in a friendly and collaborative team environment; then we are looking forward to meeting you.

• Minimum 1,5 years of independent monitoring experience in international Pharma/CRO company
• Experience in Oncology preferred but not a must; although you should be willing to work on Oncology studies
• Experience in interventional studies
• Excellent understanding of Serious Adverse Event (SAE) reporting
• Fluent in English and Polish

Learn more about our EEO & Accommodations request here.