Clinical Research Associate I

Summary

Join Precision for Medicine, Oncology and Rare Disease, a unique CRO with high CRA retention rates, as a Clinical Research Associate I/II in Poland. You will focus on 1-2 studies, becoming a protocol expert with reasonable travel and work-life balance. Your contributions will be valued, and your voice will be heard within a smaller CRO structure. You will monitor clinical studies, ensuring compliance with protocols and regulations. The role involves coordinating study setup and monitoring activities, including investigator identification and regulatory submissions.

Requirements

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
• At least one year of CRA experience (including 6 months of independent monitoring) within the CRO or pharmaceutical industry
• 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
• Experience in oncology

Responsibilities

• 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
• 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.)

Preferred Qualifications

Study start up activities experience