Precision for Medicine is looking to hire a Clinical Research Associate II to monitor and manage clinical studies at investigative sites, ensuring compliance with protocols, SOPs, ICH-GCP, and regulations. The role aims to support the company's mission in advancing precision medicine, particularly in oncology research.
Requirements
- 2 (two) years or more as a CRA in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies.
- Site management or equivalent experience in clinical research
- Oncology experience
- CRA Certification holder
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
- This is a remote based position (homebased anywhere in Italy), with travel to sites for monitoring visits.
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
- Fluency in English and for non-English speaking countries the local language of country where position based
- Please, apply in English.
