Precision for Medicine, Oncology and Rare Disease is looking to hire a Clinical Research Associate I in Poland to manage and monitor clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations. The role aims to contribute to the company's mission of advancing precision medicine in oncology and rare diseases.
Requirements
- At least six months of CRA experience (including 6 months of independent monitoring) within the CRO or pharmaceutical industry
- Experience in oncology and pulmonology studies
- Study start up activities experience
Responsibilities
- You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
- You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
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.
