(Senior) Start-up CRA, Poland
Pharmaceutical Product Development (PPD)
Warszawa PL Trinity Park III, Warsaw, PL
2 d. temu

Currently we’re looking for an experienced professional to join us on the position of :

Start-up Clinical Research Associate, Poland

The successful candidate will be primarily tasked to set up and monitor clinical trials conducted as part of international projects.

The opportunity is suitable for a professional with proven experience on a similar position.

Main accountabilities :

  • Determine protocol and regulatory compliance on the sites;
  • Perform and coordinate all aspects of the clinical monitoring process from "start up" to "close out";
  • Thrive in multi-national project teams and be focused on delivering exemplary levels of customer service;
  • Conduct monitoring activities independently.
  • Currently we’re looking for an experienced professional to join us on the position of :

    Start-up Clinical Research Associate, Poland

    The successful candidate will be primarily tasked to set up and monitor clinical trials conducted as part of international projects.

    The opportunity is suitable for a professional with proven experience on a similar position.

    Main accountabilities :

  • Determine protocol and regulatory compliance on the sites;
  • Perform and coordinate all aspects of the clinical monitoring process from "start up" to "close out";
  • Thrive in multi-national project teams and be focused on delivering exemplary levels of customer service;
  • Conduct monitoring activities independently.
  • Education and Experience :

  • Degree in pharmacy, life science or related field;
  • Ideally 2 or more years of monitoring experience in interventional studies with a CRO, pharmaceutical or biotech company.
  • Additional Requirements :

  • Demonstrated clinical trial monitoring skills;
  • In-depth understanding of ICH / GCP guidelines;
  • Excellent standard of verbal and written communication skills in English language;
  • Highly organized with strong attention to detail and deadlines;
  • Advanced skills across all of the MS Office packages;
  • Willingness to travel.
  • As an equal opportunity employer, PPD believes that employees are the key to its success, and is committed to your professional growth.

    We offer an attractive salary, comprehensive benefits package as well as bespoke personal development and training programs.

    Education and Experience :

  • Degree in pharmacy, life science or related field;
  • Ideally 2 or more years of monitoring experience in interventional studies with a CRO, pharmaceutical or biotech company.
  • Additional Requirements :

  • Demonstrated clinical trial monitoring skills;
  • In-depth understanding of ICH / GCP guidelines;
  • Excellent standard of verbal and written communication skills in English language;
  • Highly organized with strong attention to detail and deadlines;
  • Advanced skills across all of the MS Office packages;
  • Willingness to travel.
  • As an equal opportunity employer, PPD believes that employees are the key to its success, and is committed to your professional growth.

    We offer an attractive salary, comprehensive benefits package as well as bespoke personal development and training programs.

    0 : :

    Zgłoś tę pracę
    checkmark

    Thank you for reporting this job!

    Your feedback will help us improve the quality of our services.

    Aplikuj
    Mój adres email
    Klikając przycisk "Kontynuuj", wyrażam zgodę neuvoo na przetwarzanie moich danych i wysyłanie powiadomień e-mailem, zgodnie z zasadami przedstawionymi przez neuvoo. W każdej chwili mogę wycofać moją zgodę lub zrezygnować z subskrypcji.
    Kontynuuj
    Formularz wniosku