Open to opportunities

Magdalena Satała

@magdalenasataa

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Clinical Research Coordinator dedicated to advancing medical research.

Poland

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What I'm looking for

I seek a role that fosters professional growth in clinical research, emphasizing collaboration and innovation.

I am a Clinical Research Coordinator with a strong commitment to advancing medical research and ensuring patient safety. Currently, I collaborate with Principal Investigators, Monitors, Vendors, and Sponsors at Centrum Medyczne Plejady in Kraków, where I facilitate daily trial activities and ensure compliance with research protocols. My role involves monitoring patient safety throughout studies, promptly reporting adverse events, and serving as the primary contact for Clinical Research Associates during site visits.

Previously, I supported clinical trial activities as a Study Coordinator Assistant, where I managed trial documentation in accordance with ICH-GCP standards and assisted in patient visit preparations. My internship experiences have equipped me with a solid understanding of clinical trial workflows, data entry, and GCP standards, enhancing my professionalism and attention to detail. I am passionate about contributing to the field of clinical research and continuously improving my skills.

Experience

Work history, roles, and key accomplishments

Current

Clinical Research Coordinator

Current

Centrum Medyczne Plejady

Oct 2024 - Present (9 months)

Collaborated with Principal Investigator, Monitors, Vendors, and Sponsors to facilitate daily trial activities and comply with research protocols. Monitored patient safety throughout the study, promptly reporting Adverse Events and Serious Adverse Events.

Clinical Research Patient Safety Adverse Events Vendor Management

Study Coordinator Assistant

Centrum Medyczne Plejady

Jul 2023 - Present (2 years)

Supported the Clinical Research Coordinator in managing clinical trial activities and ensuring protocol compliance. Assisted in managing trial documentation in accordance with ICH-GCP and local regulatory standards.

Clinical Trial Management ICH GCP Regulatory Clinical Trial Documentation Veeva Inform

Clinical Data Review and Query Resolution Internship

Małopolskie Badania Kliniczne Sp. z o.o.

Jul 2022 - Present (3 years)

Gained knowledge of clinical trial workflow, data entry, and GCP standards. Became familiar with Electronic Data Capture (EDC) systems and the Informed Consent process.

Data Entry GCP EDC

Pharmacy Technician

Ziko Apteka | Apteka Słoneczna

Sep 2017 - Present (7 years 10 months)

Provided day-to-day support in dispensing prescription and OTC medications. Advised patients on proper medication use, potential interactions, and basic health-related questions.

Patient Counseling Pharmacy Operations Prescription Pharmaceutical Standards