Cra Ii/ Scra

pfm; Polska; Remote; PLN 120,000 - 180,000; Full time

Job summary

Precision for Medicine is recruiting a Clinical Research Associate II / Senior CRA to join our fully home-based team in Poland. You will independently monitor investigative sites, ensure patient safety, data integrity and study delivery, and collaborate with CTMs and study teams to drive timely resolutions.

Ideal candidates have 3+ years of independent monitoring in CRO/pharma, oncology experience, and fluency in Polish and English.

Qualifications

• 3+ years of independent monitoring experience within CRO/pharma.
• Experience monitoring oncology clinical trials.

Responsibilities

• Independently monitor investigative sites, owning site performance, quality and risk identification from initiation to close-out.
• Collaborate with CTMs and study teams to anticipate issues, drive timely resolution, and ensure studies are conducted and reported per protocol and regulatory requirements.
• Interact with clients and support site payment activities as needed.

Skills

Independent monitoring

Oncology monitoring

Education

Science/Healthcare degree

Job description

Precision for Medicine 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.

Our CRAs work with a manageable study portfolio, allowing them to build deep protocol and site knowledge rather than spreading their focus across too many studies. With reasonable travel expectations, accessible line management and a smaller CRO environment, experienced CRAs have the autonomy to make decisions, influence how studies are delivered and see the impact of their work.

Precision for Medicine is recruiting a Clinical Research Associate II / Senior Clinical Research Associate to join our full-service team in Poland.

This position is fully home based

About you:

• You are an experienced independent monitor who takes ownership of your sites and does not wait to be told what needs attention.
• You understand what really matters for patient safety, data integrity and study delivery, and can distinguish critical risks from administrative noise.
• You build credible relationships with investigators and site teams while remaining confident in addressing difficult or sensitive issues.
• You identify emerging risks early, escalate appropriately and come with solutions, not just problems.
• You are organized and well prepared, able to manage competing priorities across your sites without compromising quality.
• You communicate clearly with CTMs and study teams and can confidently represent the site perspective in project discussions.
• You take responsibility for the quality and outcomes of your work.

How we will keep you busy and support your growth:

• You will independently manage and monitor investigative sites, taking ownership of site performance, quality and risk identification from site initiation through close-out.
• You will partner closely with CTMs and study teams to anticipate issues, drive timely resolution and ensure studies are conducted, recorded and reported in accordance with the protocol, SOPs, ICH-GCP and applicable regulatory requirements.
• You may also interact directly with clients and support site payment activities.
• Depending on your experience, you may have the opportunity to mentor less experienced CRAs and contribute your expertise to study-level discussions and process improvements.

Qualifications:

Minimum Required:

• 3+ years of independent monitoring experience within the CRO or pharmaceutical industry.
• Independent monitoring experience in oncology clinical trials.

Other Required:

• Availability for domestic travel, including overnight stays, which may constitute up to approximately 50-60% travel commitment; occasional international travel may be required.
• Fluency in Polish and English.

Preferred:

• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline.
• Experience monitoring complex early-phase oncology studies, including Phase I and/or CAR-T trials.

Why Precision for Medicine?

Precision's uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.

Precision for Medicine is revolutionizing the attack on cancer-and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions-and optimize the oncology development pathway.

We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive changes for the company.

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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [e-mail].