Remote opportunity at
pfm medical, inc.CRA II/ SCRA
Precision for Medicine seeks a CRA II or Senior Clinical Research Associate to operate on a full-time, fully home-based schedule in Poland. The organization functions as…
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About This Role
Precision for Medicine seeks a CRA II or Senior Clinical Research Associate to operate on a full-time, fully home-based schedule in Poland. The organization functions as a specialized contract research organization focused on oncology and rare diseases, utilizing advanced biomarker and data analytics solutions to support targeted clinical trials. This position suits an experienced, independent monitor who prioritizes patient safety, data integrity, and protocol compliance while maintaining a manageable study…
Job Description
Precision for Medicine seeks a CRA II or Senior Clinical Research Associate to operate on a full-time, fully home-based schedule in Poland. The organization functions as a specialized contract research organization focused on oncology and rare diseases, utilizing advanced biomarker and data analytics solutions to support targeted clinical trials.
This position suits an experienced, independent monitor who prioritizes patient safety, data integrity, and protocol compliance while maintaining a manageable study portfolio. The role offers reasonable travel expectations and the opportunity to exercise autonomy in site management, risk identification, and study delivery.
Selected candidates will oversee investigative sites from initiation through close-out, collaborate with clinical trial managers, communicate with study teams, and potentially mentor less experienced colleagues or interact directly with clients.
Responsibilities
- Manage and monitor investigative sites independently from initiation through close-out
- Partner with clinical trial managers and study teams to identify risks and resolve issues promptly
- Ensure trials adhere strictly to study protocols, standard operating procedures, ICH-GCP guidelines, and applicable regulations
- Interact directly with clients and assist with site payment activities as needed
- Mentor junior clinical research associates and contribute to study-level discussions and process improvements depending on experience
Requirements
- Minimum of three years of independent monitoring experience within a CRO or pharmaceutical industry setting
- Demonstrated independent monitoring experience specifically in oncology clinical trials
- Availability for domestic travel including overnight stays of approximately 50 to 60 percent, alongside potential occasional international travel
- Professional fluency in both Polish and English
- Legal authorization to work in the country of employment without requiring employer sponsorship
Qualifications
- Graduate or postgraduate degree with a focus in a scientific or healthcare discipline
- Prior 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, the posting explicitly states that the position is fully home-based in Poland.
What is the travel requirement for this role?
The job requires domestic travel including overnight stays of approximately 50 to 60 percent, and may also require occasional international travel.
What experience is required to apply?
Candidates must have a minimum of three years of independent monitoring experience within the CRO or pharmaceutical industry, specifically including independent monitoring experience in oncology clinical trials.
What languages must applicants speak?
Applicants must be fluent in both Polish and English, and applications are requested to be submitted in English.
Does the posting specify salary or benefits?
No, the job posting does not provide details regarding salary or employee benefits.
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