Remote CRA II

Summary

Join us at Precision for Medicine, where we integrate clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences. We're passionate about cultivating our culture and proud of our high CRA retention rates. As a CRA, you'll have a lower than average number of protocols, reasonable travel, and a great work-life balance.

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.)