Precision for Medicine, Oncology and Rare Disease is looking to hire Clinical Research Associate I/ Clinical Research Associate II in Poland to manage and monitor clinical studies, ensuring compliance with protocols and regulations, and to contribute to the company's mission of advancing precision medicine in oncology and rare diseases.
Requirements
- At least one year of CRA experience (including 6 months of independent monitoring) within the CRO or pharmaceutical industry
- Experience in oncology
- Study start up activities experience
Responsibilities
- Monitor and own the progress of clinical studies at investigative sites
- Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
- Coordinate all necessary activities required to set up and monitor a study
- Identify investigators
- Help prepare regulatory submissions
- Conduct pre-study and initiation visits
Other
- You are calm, thoughtful, and responsive when things don’t go as planned.
- You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
- You find quick and creative ways of overcoming difficulties.
- You have an impeccable eye for detail.
- You identify potential study risks and propose solutions on how to mitigate them.
- You take responsibility in the quality and outcomes of your work.
- You are adept at handling conflict by using tried and true resolution strategies.
- Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
- Fluency in English and for non-English speaking countries the local language of country where position based
