drjobs Senior Clinical Research Associate Sponsor dedicated in POLAND

Senior Clinical Research Associate Sponsor dedicated in POLAND

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1 Vacancy
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Job Location drjobs

Warsaw - Poland

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Are you interested in collaborating with leading pharma companies to help patients all around the world

When you join IQVIA as a sponsordedicated Senior CRA in Poland youll enjoy the stability and resources of a leading global contract research organization while gaining direct experience with one of our clients. Whether youre just starting out or looking to deepen your expertise this role promises to offer intentional career growth and professional development. With access to worldclass training and mentoring youll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.

Your responsibilities will include:

  • Performing site selection initiation monitoring and closeout visits
  • Supporting the development of a subject recruitment plan
  • Evaluating the quality and integrity of site practices in accordance with regulatory requirements i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Managing progress by tracking regulatory submissions recruitment case report form (CRF) completion and data query resolution
  • Collaborating with experts at study sites and with client representatives
  • Depending on client model there might be remotemonitoring involvement in study startup processes specialization on therapeutic area (pharmaceutical product or medical devices)

Qualifications:

  • University Degree in life science or other scientific discipline or apprenticeship in health care
  • Minimum of 3 years of onsite monitoring experience alternatively an equivalent combination of education training and experience
  • Strong experience in monitoring of clinical trials
  • Knowledge of applicable clinical research regulatory requirements i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Strong written and verbal communication skills attention to detail and ability to work in a fast pace environment
  • Good command of Polish and English language
  • Flexibility to travel

What you can expect:

  • Resources that promote your career growth
  • Leaders that support flexible work schedules
  • Programs to help you build your therapeutic knowledge
  • Dynamic work environments that expose you to new experiences
  • Homeoffice company car and more

Whatever your career goals we are here to ensure you get there!

We invite you to join IQVIA.

Please apply with your English CV.

#CRASDAJD #CRA #SCRA #SeniorCRA#iqvia

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at


Required Experience:

Senior IC

Employment Type

Full-Time

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