Remote CRA II

Summary

Join Precision for Medicine, a unique CRO that integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences. We offer a culture of passion, high CRA retention rates, and a lower-than-average number of protocols. As a Clinical Research Associate (CRA), you will monitor and own the progress of clinical studies at investigative sites, ensuring compliance with regulations and standards.

Requirements

• College degree or equivalent experience
• At least 2 years independent on-site monitoring experience within the CRO or Pharmaceutical industry
• Oncology experience is essential
• 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

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.)