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Site Research Assistant - Poznań

Iqvia

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Yesterday

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Location
Warsaw, Poland
Workplace
Onsite
Type
Part-time
Department
Education
Experience
2+ years
Source
Workday

Description

Site Research Assistant in Poznań

Working Hours: 15-20h per week

Start Date: Immediately
Duration: Approximately 5 months


IQVIA is currently recruiting a dedicated Site Research Assistant to support a clinical research site in Poznań .This 15-20h hour per week role offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.


Key Responsibilities

As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:


  • Prescreening and Screening tasks
  • Contacting patients by phone and vrifying inclusion and exclusion criteria
  • Scheduling patient visits
  • Coordinating further pre-screening (preSCR) visits
  • Contacting and reassessment of previous patients
  • Supporting continued patient engagement and follow-up
  • External outreach to other centers to inform them about the ongoing study and encourage referral of potential patients
  • Communicating with study monitors and responding to study-related inquiries
  • Carrying out general administrative tasks related to the study

Your Profile
We are looking for candidates who bring a combination of education, experience, and skills:

  • Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)
  • Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
  • Good knowledge of medical terminology
  • Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
  • Must have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
  • Excellent interpersonal and communication skills
  • Strong organizational skills and attention to detail



Why Join IQVIA?
At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.


Interested?
If this sounds like the right opportunity for you, we encourage you to apply today.



#LI-HCPN

#LI-CES

#LI-DNP

#LI-NS

#LI-Onsite

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 https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is zł83,000.00 - zł154,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Skills

ExcelClinical Trials

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