Clinical Research Associate II

Summary

Join Precision for Medicine, a CRO with high CRA retention rates, offering a unique work environment. You will have a manageable workload, reasonable travel, and a strong work-life balance. Your voice will be heard, and you'll have a significant impact. This Clinical Research Associate II position is based in Madrid or Barcelona. You will monitor clinical studies, ensuring compliance with protocols and regulations. The role involves coordinating study setup and monitoring activities.

Requirements

• 4-year college degree or equivalent experience
• 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
• 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
• Candidates must reside in Madrid or Barcelona

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

Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline