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Field Clinical Specialist

  • Warszawa, mazowieckie
  • Specjalista
  • 03.01.2019

    Pracodawca ma prawo zakończyć rekrutację we wcześniejszym terminie.

    Abbott Medical, a world leader in the medical industry, is looking for candidates for the position:

    Field Clinical Specialist
    Miejsce pracy: Warszawa


    PURPOSE OF THE JOB:
    As a Field Clinical Operation Specialist, ensure that assigned clinical projects are planned, conducted and progress/results communicated in compliance with relevant local, national and international clinical trial regulations/guidelines and with the highest standard of quality defined by Company Standard Operating Procedures (SOPs) and by Good Clinical Practice.


    Main
    Responsibilities:

    • Coordinate, implement, execute and support all the assigned Clinical Projects
    • Facilitate/support adequate site activation times, enrollment rate and data quality with regular and frequent visits to the assigned centers
    • Take proactive measures to ensure site activation and project enrollments within timelines and defined forecasts
    • Coordinate timely and quality data collection
    • Arrange ad-hoc meetings or activities for data quality improvement
    • Guarantee data quality through periodic reporting on CRF status, site compliance and regular visits to the centers
    • Ensure compliance in safety reporting
    • Guarantee periodic communication to ECs and CA according to the applicable legislation (if applicable) and be responsible of the correct study documents archiving
    • Coordinate or perform (when applicable) site compliance, data quality activities, and monitoring activties in cooperation with the Field CRA
    • Communicate internally on project progress to stakeholders
    • Develop/coordinate/execute action Plans and collect all projects associated documents
    • Identify and qualify appropriate study sites, physicians and staff in accordance with all internal stakeholders and SOPs.
    • Train field people assigned to projects
    • Ensure project products availability and traceability (if applicable)
    • Ensure study/country/center specific essential documents are generated and filed in project administrative binders/OC database and project folders on internal network
    • Define requirements and coordinate service providers (if applicable)
    • Coordinate and communicate regularly with Investigators and Steering Committee / Adjudication committee / DSMB members
    • Ensure proper communication between the Investigators and BCC/US for sub analysis, publications and data management for Global projects
    • Take active role in presenting clinical activities in local internal and external meetings
    • Coordinate data analysis for local projects (when applicable)
    • Be the clinical reference point for local clinical activities in the assigned area (when applicable)

    Background:

    • 3-5 years of experience in clinical projects, as project leader or CRA, in medical device, biotech or pharmaceuticals industry/CRO
    • Medical/biomedical/bioengineer/bioscience/scientific background (MS/BS/Engineer/PhD/MD, etc) or relevant previous experience

    Abilities:

    • Excellent communication, prioritization, organizational and time management skills
    • Team player with positive constructive attitude to solve problems. Eager to learn, stress resistant
    • Strong self-development abilities and able to work independently
    • Strong ability in working with the health care professional
    • Fluency in English (both written and verbal), any other European/local language is an asset
    • Ability to travel up to 70 %

    What we offer:

    • Flexible working hours
    • Private medical care  (Medicover)
    • Life insurance
    • Fresh fruits everyday 😊
    • Coffee every day 😊
    • Friendly Environment
    • Multicultural Environments
    • Stable contract
    • Working tools

    Interested candidates please send the CV in English.

    Please be advised that we will only contact selected persons.

    Wyrażam zgodę na przetwarzanie przez ogłoszeniodawcę moich danych osobowych, zawartych w mojej ofercie pracy, dla potrzeb niezbędnych do realizacji procesu rekrutacji zgodnie z ustawą z dnia 29 sierpnia 1997 r. o ochronie danych osobowych (t.j. Dz. U. z 2016 r., poz. 922). Jednocześnie wyrażam zgodę na przetwarzanie przez ogłoszeniodawcę moich danych osobowych na potrzeby przyszłych rekrutacji.