Summary
Overview
Work History
Education
Skills
Languages
Additional Information
Timeline
Generic
MARTYNA DZIK

MARTYNA DZIK

Chorzów

Summary

Experienced Clinical Research Coordinator with over 3 years of experience in clinical trials. In additional second professional area is role of laboratory diagnostician. Ambitious, multi-tasking, willing to expand knowledge in the field of clinical trials and further development.

Overview

3
3
years of professional experience

Work History

Senior Clinical Research Coordinator

Pratia Hematologia SP. Z O.O.
12.2021 - Current
  • Coordination of phase I-IV clinical trials in the hemato-oncology field (following indications: multiple myeloma, mielofibrosis, CLL/SLL, DLBCL, polycythemia vera and thrombocytopenia).
  • Supervision over the accuracy conducting of the clinical trials in accordance with study protocol and GCP rules.
  • Ensuring completeness of study documentation (ISF, source documentation, logs).
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Timely entry of source data in eCRF and queries resolving.
  • Adverse event (AE/SAE) reporting.
  • Assigning of study drugs in IXRS systems.
  • Efficient cooperation with site team (Subinvestigators, Study Nurses, Pharmacists, Study Coordinators), with CRAs/CTAs and sponsor's representatives.
  • Worked with study vendors - central and local laboratories, medical imaging departments etc.
  • Conducting electronic questionnaires with patient (ePRO, e-diaries).
  • Prepared a templates for all type of visits per protocol and lab manual.
  • Interpreted of patient's laboratory results.
  • Participated in initiation visits, regular monitoring visits, close-out visits, audits visits and investigator meetings.
  • Identified issues, analyzed information and provided solutions to problems.
  • Managed time efficiently in order to complete all tasks within deadlines.

Team Leader

Pratia Hematologia SP. Z O.O.
01.2023 - Current
  • Training new employees in coordinating clinical trials and sharing of knowledge with juniors.
  • Monitored team performance and provided constructive feedback to maintain quality standards.
  • Worked with team to identify areas of improvement and devised solutions based on findings.
  • Verified of study documentation in terms of quality and compliance.

Hyggio Global Coordinator

Pratia Hematologia SP. Z O.O.
05.2023 - Current
  • Set up of new study protocols and additional procedures in Hyggio [CTMS & eTMF].
  • Supported the study site team with Hyggio functionality.
  • Cooperation with Clinical Trials Finance Department.

Clinical Research Coordinator

Holsa Clinical - Gyncentrum SP. Z O.O.
08.2020 - 12.2021
  • Coordination of phase II-IV clinical trials in the dermatology field (following indications: atopic dermatitis, onychomycosis, hand eczema, psoriasis).
  • Supervision over the accuracy conducting of the clinical trials in accordance with study protocol and GCP rules.
  • Ensuring completeness of study documentation (ISF, source documentation, logs).
  • Maintained compliance with protocols covering patient care and clinical trial operations.
  • Timely entry of source data in eCRF and queries resolving.
  • Adverse event (AE/SAE) reporting.
  • Assigning of study drugs in IXRS systems.
  • Efficient cooperation with site team (Subinvestigators, Study Nurses, Pharmacists, Study Coordinators), with CRAs/CTAs and sponsor's representatives.
  • Worked with study vendors - central and local laboratories, medical imaging departments etc.
  • Conducting electronic questionnaires with patient (ePRO, e-diaries).
  • Prepared a templates for all type of visits per protocol and lab manual.
  • Participated in initiation visits, regular monitoring visits and close-out visits.
  • Gathered, processed, and shipped lab specimens.
  • Ordered a study supplies - laboratory kits, waybills, dry ice etc.
  • Conducted and monitored a temperature logs.
  • Created a medical content and education videos about clinical trials on site's website.
  • Supported in start-up process of new studies.
  • Managed time efficiently in order to complete all tasks within deadlines.
  • Identified issues, analyzed information and provided solutions to problems.

Laboratory Diagnostician

Samodzielny Publiczny Szpital Kliniczny Im. A. Mielęckeigo W Katowicach
01.2021 - 03.2021
  • Performed laboratory assessments - general analytics, clinical chemistry, immunochemistry, hematology, serology and microbiology.
  • Calibrated of laboratory equipments.
  • Interpreted of results, assessment of microbiological cultures and evaluation of peripheral blood slides.

Education

Master of Science - Medical Analytics

Medical University of Silesia
Katowice
08.2021

No Degree - ICH GCP E6(R2)

The Global Health Network
08.2020

No Degree - "Clinical Trials Monitoring Basics"

Soft Communication
07.2020

No Degree - Course "Thrombocytopenia - Pathogenesis, Diagnosis

Medical University of Silesia
Katowice
04.2022

No Degree - Course Online For Lab. Diagnosticians

Roche Diagnostics Academy
03.2022

No Degree - "Basic Life Support"

American Heart Association
05.2021

No Degree - "Innovations in Oncology"

Medical University of Silesia
03.2019

Skills

  • Knowledge of ICH GCP E6(R2)
  • English - advanced level
  • Familiar with following systems - iMedidata, Rave, VeevaVault, Trialmax, Clario, Inform, Suvoda, Oracle, Impala, Lilly, Endpoint
  • Fluent of Microsoft Office
  • Driving licence - cat B
  • Medical copywriter
  • Ability to work independently and teamwork
  • Easily communication skills
  • Analytical thinking skills
  • Responsibility
  • Task prioritizing
  • Good adaptability
  • Accuracy and timeliness in performing tasks
  • Problem-solving abilities
  • Regulatory Requirements
  • Medicine, Clinical Trials

Languages

Polish
Native language
English
Advanced
C1

Additional Information

I consent to the processing of my personal data for the purpose of recruitment for the position to which I am applying.

Timeline

Hyggio Global Coordinator

Pratia Hematologia SP. Z O.O.
05.2023 - Current

Team Leader

Pratia Hematologia SP. Z O.O.
01.2023 - Current

Senior Clinical Research Coordinator

Pratia Hematologia SP. Z O.O.
12.2021 - Current

Laboratory Diagnostician

Samodzielny Publiczny Szpital Kliniczny Im. A. Mielęckeigo W Katowicach
01.2021 - 03.2021

Clinical Research Coordinator

Holsa Clinical - Gyncentrum SP. Z O.O.
08.2020 - 12.2021

Master of Science - Medical Analytics

Medical University of Silesia

No Degree - ICH GCP E6(R2)

The Global Health Network

No Degree - "Clinical Trials Monitoring Basics"

Soft Communication

No Degree - Course "Thrombocytopenia - Pathogenesis, Diagnosis

Medical University of Silesia

No Degree - Course Online For Lab. Diagnosticians

Roche Diagnostics Academy

No Degree - "Basic Life Support"

American Heart Association

No Degree - "Innovations in Oncology"

Medical University of Silesia
MARTYNA DZIK