Clinical Research Associate I/II

Summary

Join Precision for Medicine, a CRO with high CRA retention rates, offering a unique work environment. You'll enjoy a lower-than-average protocol workload, reasonable travel, and a strong work-life balance. Your voice will be heard, and you'll have a significant impact. This fully remote position (based in Madrid or Barcelona) is for a CRA I or CRA II. The role involves monitoring clinical studies, ensuring compliance, and coordinating study activities. Precision offers a supportive and collaborative culture where your contributions are valued.

Requirements

• 4-year college degree or equivalent experience
• At least 1 year of monitoring experience within the CRO or pharmaceutical industry
• 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
• 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

Benefits

• Fully home-based position
• Lower than average number of protocols
• Reasonable travel
• Strong work/life balance
• Your voice will be heard and you will have influence and impact
• Support from direct line management