Višnja Bukarica

Regional Site Manager Lead at ERGOMED
  • Claim this Profile
Contact Information
us****@****om
(386) 825-5501
Location
Serbia, RS
Languages
  • English Professional working proficiency
  • German Elementary proficiency
  • Croatian Native or bilingual proficiency

Topline Score

Topline score feature will be out soon.

Bio

Generated by
Topline AI

5.0

/5.0
/ Based on 2 ratings
  • (2)
  • (0)
  • (0)
  • (0)
  • (0)

Filter reviews by:

zdenka selendic

I highly recommend Visnja Bukarica as a candidate for employment. We have been working closely for several years now. Visnja has excellent communication skills. In addition, she is extremely organized, reliable and computer literate. She can work independently and is able to follow through to ensure that the job gets done. She is flexible and willing to work on any project that is assigned to her. Visnja would be a tremendous asset for your company and has my highest recommendation.

Marija Flego

I have been working with Visnja on several projects in past 5 years. Visnja is responsible, reliable and very organize. She has been working on all phases of the study, from the start up of the trial until close out and archiving, and has past successfully both internal and external audits.I would highly recommend Visnja as she has a great experience and knowledge in clinical trials.

You need to have a working account to view this content.
You need to have a working account to view this content.

Experience

    • United Kingdom
    • Pharmaceutical Manufacturing
    • 300 - 400 Employee
    • Regional Site Manager Lead
      • Apr 2022 - Present

    • Senior Site Manager
      • Feb 2017 - Apr 2022

    • United Kingdom
    • Pharmaceutical Manufacturing
    • 300 - 400 Employee
    • Site Manager
      • Oct 2013 - Feb 2017

    • United Kingdom
    • Pharmaceutical Manufacturing
    • 300 - 400 Employee
    • CRA
      • Jun 2010 - Feb 2013

      -main line of communication between the sponsor and Investigator-site start-up and Initiation-verification that the conduct of the study is in compliance with the currently approved Protocol ,GCP and with the applicable RA requirements-verification that the rigts and well-being of human subjects are protected-verification that the Study Team have adequate qualifications and resources and do theysafely and prroperly conduct the study throughhout the Protocol-verification of source documentation and CRF verification of IMP and other study materials-reporting status to PM-query resolution-site close-out and TMF archiving Show less

    • Site Manager
      • Sep 2007 - Feb 2013

      -Fesibility/Site Identification-Study Start Up-Site Start Up- Managing of recruitment-Managing of all on-site needed staf-On-Site Management-In-House Site Management-Team nad Investigator Meetings,TC-Administration-Communication with Investigators, EC, RA, CRA, PM and Sponsor-Preparing PowerPoint presentation for Site Investigational team and continuously education on Site

    • CTA/Site Manager/CRA
      • Mar 2007 - Feb 2013

    • CTA/RA assistant
      • Mar 2007 - Apr 2009

      CTA/PM assistant at Ergomed CRO:-assistance to Clinical Trials-administrative activities and support-archiving of study related documents-assistance in the submmission to relevant EC and RA and communication with them/inform monitor,PM,Sponsor about-assistance to PM and CRAs-setting up Investigator Site Files-archiving Trial Master File

    • a nurse-anesthetist
      • Jan 1992 - Mar 2007

    • a nurse at cardiovaskular surgical department
      • Apr 2004 - Dec 2006

Education

  • High School of Health and Social Work of St. Elizabeth, Bratislava, Slovakia
    Hospital and Health Care Facilities Administration/Management, BCs degree
    2017 - 2020
  • Secondary medical school, Zadar
    High school
    1986 - 1990

Community

You need to have a working account to view this content. Click here to join now