Clinical Research Associate I/II - Remote

Overview

Precision for Medicine, Oncology and Rare Disease is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages. We are now recruiting Clinical Research Associate I/ Clinical Research Associate II to join our team in Poland.

CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will focus on an average of one to two studies setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.

In Short

• Monitor and own the progress of clinical studies at investigative sites.
• Ensure clinical studies are conducted per protocol, SOPs, ICH-GCP, and regulations.
• Coordinate activities for study setup and monitoring.
• Identify investigators and assist with regulatory submissions.
• Conduct pre-study and initiation visits.
• Travel commitment may be up to 50-60%.
• Fluency in English and local language required.
• Experience in oncology is preferred.
• Work in a supportive environment with high CRA retention rates.
• Contribute to impactful clinical research.

Requirements

• Graduate or postgraduate degree in a scientific or healthcare discipline.
• At least one year of CRA experience, including independent monitoring.
• Availability for domestic travel, including overnight stays.
• Detail-oriented and adept at conflict resolution.
• Impeccable eye for detail and ability to identify study risks.

Benefits

• Supportive work environment with high retention rates.
• Opportunity to impact clinical research positively.
• Work/life balance with reasonable travel commitments.
• Direct influence on projects and support from management.