other
Posted 18 hours agoCRA2
at Fortrea
Warsaw, PolandOn-site
Responsibilities
- 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 Responsible for all aspects of registry management as
Requirements
- Qualifications: 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.
- 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 Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials.
Contact
- For more information about Fortrea, visit www.fortrea.com .
Additional details
- With over 15,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
- We are currently recruiting for our multisponsor team in central 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.
- Responsibilities include but are not limited to: 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 materials and instructions to safely enter patients into the
- requirements are adhered to according to the applicable regulatory
- 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 Education and
- 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.
- Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.
- Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
- Fortrea is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind.