Clinical Research Associate I

Summary

Join Precision for Medicine, Oncology and Rare Disease, a 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. Travel is reasonable, ensuring work-life balance. Your contributions will be valued, and you will have a voice in a smaller CRO setting. The role involves monitoring clinical studies, ensuring compliance with regulations, and coordinating study setup activities. You will be responsible for identifying investigators, preparing regulatory submissions, and conducting study visits.

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