Summary
Overview
Work History
Education
Skills
Certification
Timeline
RegisteredNurse

PRECIOUS ANOSHIRI MD MA

Clinical Trial Safety Scientist, Oncology
Warsaw

Summary

A qualified Medical Doctor with over 2 years of experience in clinical medicine and Trial safety majoring in Oncology. I have practical experience in study leadership with a track record in decision making, delegation, risk identification and mitigation, set up, review, and publication of study documents such as MOP, and CSP, medical data review, interpretation, and querying, using my Knowledge as a physician and skills in Medical Review tools, query management and EDC systems. Possessing emotional and social intelligence having collaborated in cross-cultural environments. I am confident that I will bring value to the team.

Overview

4
4
years of professional experience
10
10
years of post-secondary education
4
4
Certifications
4
4
Languages

Work History

Clinical Trial Safety Scientist

AstraZeneca Polska
Warsaw
04.2022 - Current
  • Led two priority KPI, extended Scope Late phase Oncology studies as the Point of Contact (POC)
  • Overseeing the study state, ensuring that we meet KPI, ensuring that we meet timelines and deliverables, identifying potential risks, mitigating such risks, delegating responsibilities within the team, participating and representing the Global Trial Safety Review Center (TRISARC) in stakeholder meetings, reviewed team performance, tracking study metrics using EDC system query Management tools, and provided study team leadership
  • Provided backup to the Scientist Associate Directors (SADs) and support to the global medical teams, including but not limited to the Senior Global Development Medical Director (Study Physician), Global Development Scientist Director, and Global Clinical Program Lead, among others
  • Collaborated with other stakeholders of the Core and Extended Teams, such as Centralized Monitoring (Risk Based Quality Management, RBQM), Data Management, SMM, GCS – IRT, Regulatory Affairs, Study Statisticians, and GST, among others
  • Mentored and trained onboarding Scientists and Senior Scientists, and constantly provided support to my teammates
  • Reviewed a Large amount of clinical trial safety data in extended and standard scopes using medical review tools and EDC, checking for logical and medical consistency, and clarifying discrepancies via queries, making Important Medical Escalations (IMEs) to the Global Medical Team
  • Followed up with Sites via the signed CRA/site monitor to ensure medical data consistency, and with the support of the study physician, the retraining of site staff
  • Reviewed Global Physicians Report (GPR) on monthly bases for medical consistency, while supporting DM for data coherence as part of the extended scope
  • Reviewed the Logic and performed User Acceptance Testing (UAT) for my programmed listings as part of my extended scope
  • Set up, reviewed, and published the Medical Oversight Plan (MOP) for one of my studies
  • Supported the Study Physician and Medical Scientists in preparing Clinical Study Report narratives for an Independent Data Monitoring Committee (IDMC)
  • Created and presented Clinical Study Reports for the monthly Study Safety Period Review (SSPR) with the Core and Extended Team Stakeholders, taking the meeting minutes and uploading them on the eTMF
  • Created a departmental Hub for POCs, to aid knowledge sharing, process standardizations, and providing better study leadership, thus, meeting the departmental goals
  • Helped create and led an Employee Resource Group (ERG) for a minority group on the site.

FNOL Specialist

LYFT
Warsaw
12.2019 - 03.2022
  • Mentored and trained onboarding specialists on the department and company SOPs
  • Reviewed large data identifying discrepancies and reconciling when applicable
  • Analyzed claims, assessed eligibility, and sent them for processing
  • Followed up with clients when required per SOP
  • Collaborated with internal and external stakeholders both locally and globally
  • Worked flexible hours in a hybrid-working environment

Clinical Residence

Grodno City Hospital of Emergency Care
Grodno
06.2019 - 09.2019
  • Created and reviewed Case Report Files
  • Collected anamnesis to help establish a diagnosis
  • Examined patients physically and instrumentally
  • Established preliminary diagnosis and final diagnosis under supervision
  • Assisted and performed surgical procedures under supervision
  • Presented cases and case histories at medical conferences and rounds
  • Wrote case summaries for conference and internal publications
  • Mentored and taught 3 - 5 year medical students as an assistant.

Education

Master of Arts - Accounting And Finance

AKADEMIA EKONOMICZNO-HUMANISTYCZNA W WARSZAWIE
Warsaw, Poland
10.2019 - 09.2021

M.D. - Medicine And Surgery

GRODNO STATE MEDICAL UNIVERSITY
Grodno, Belarus
09.2012 - 06.2019

No Degree - Russian Language Studies And PreMed

GRODNO STATE COLLEGE OF TECHNOLOGY
Grodno, Belarus
06.2012 - 08.2013

Skills

MultitaskingCommunication and PresentationLeadership and decision makingStakeholders CollaborationMicrosoft Apps (Excel, PowerPoint, Word, Outlook, MS SharePoint)DocuSign and AdobeClinical Trial Management System (CTMS)MedDRA & ATCIndividual Case Safety Report (ICSR)Veeva Clinical/Enterprise VaultREACT 4Power BITherapeutic Areas include Oncology, Cardiovascular, Respiratory, Immunology, Precision medicine, Endocrinology, Renal, Vaccines and vaccinology, Infectious disease, Rare diseases

Certification

Lean Six Sigma, Yellow belt

Timeline

Clinical Trial Safety Scientist

AstraZeneca Polska
04.2022 - Current

FNOL Specialist

LYFT
12.2019 - 03.2022

Master of Arts - Accounting And Finance

AKADEMIA EKONOMICZNO-HUMANISTYCZNA W WARSZAWIE
10.2019 - 09.2021

Clinical Residence

Grodno City Hospital of Emergency Care
06.2019 - 09.2019

M.D. - Medicine And Surgery

GRODNO STATE MEDICAL UNIVERSITY
09.2012 - 06.2019

No Degree - Russian Language Studies And PreMed

GRODNO STATE COLLEGE OF TECHNOLOGY
06.2012 - 08.2013
PRECIOUS ANOSHIRI MD MAClinical Trial Safety Scientist, Oncology