Remote opportunity at
Precision Medicine GroupCRA II/ SCRA
Precision Medicine Group is hiring a CRA II / Senior Clinical Research Associate to join its full-service team based in Poland. This remote position is fully…
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About This Role
Precision Medicine Group is hiring a CRA II / Senior Clinical Research Associate to join its full-service team based in Poland. This remote position is fully home-based. The organization operates as a specialized contract research organisation focusing on oncology clinical trials, utilizing advanced biomarker data and targeted adaptive trial designs. This role suits an independent professional who can manage investigative sites from initiation through close-out with manageable study portfolios and…
Job Description
Precision Medicine Group is hiring a CRA II / Senior Clinical Research Associate to join its full-service team based in Poland. This remote position is fully home-based. The organization operates as a specialized contract research organisation focusing on oncology clinical trials, utilizing advanced biomarker data and targeted adaptive trial designs.
This role suits an independent professional who can manage investigative sites from initiation through close-out with manageable study portfolios and reasonable travel expectations. Monitoring personnel handle study delivery, patient safety, and data integrity while communicating closely with clinical trial managers. Depending on individual experience levels, the position offers opportunities to mentor junior staff and contribute to process improvements.
Responsibilities
- Independently manage and monitor investigative sites from initiation through close-out
- Oversee site performance, quality, and risk identification
- Partner with CTMs and study teams to resolve issues and ensure protocol, SOP, and ICH-GCP compliance
- Interact directly with clients and assist with site payment activities
- Mentor less experienced CRAs based on background and experience
- Contribute expertise to study-level discussions and process enhancements
Requirements
- At least 3 years of independent monitoring experience within the pharmaceutical or CRO sector
- Prior independent monitoring experience in oncology clinical trials
- Availability for domestic travel, including overnight stays, up to approximately 50 to 60 percent
- Capability for occasional international travel
- Fluency in both Polish and English
- Legal authorization to work in the country of employment without employer sponsorship
Qualifications
- Graduate or postgraduate degree in a scientific or healthcare discipline
- Experience monitoring complex early-phase oncology studies, including Phase I or CAR-T trials
Core Skills
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Is this position remote?
Yes, this position is fully home-based in Poland.
What travel is required for this role?
The position requires domestic travel with overnight stays of approximately 50 to 60 percent, along with potential occasional international travel.
What experience is necessary to qualify?
Candidates must have a minimum of three years of independent monitoring experience in the pharmaceutical or CRO industry, specifically including independent oncology monitoring experience.
What is the salary for this position?
The posting does not specify the salary.
Sample Interview Questions
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