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IQVIA
Clinical Research Coordinator YorkIQVIA • London, England, UK
Clinical Research Coordinator York

Clinical Research Coordinator York

IQVIA • London, England, UK
27 days ago
Job type
  • Full-time
  • Part-time
Job description

Clinical Research Coordinator in York

Working Hours: 24 hours per week

Start Date: Immediately
Duration: Approximately 6 months

IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in York. This part-time position 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
  • Review charts from the site data base
  • Maintaining and updating study documentation including protocols case report forms (CRFs) and Electronic Data Capture (EDC) systems
  • Supporting patient screening and enrollment including handling informed consent and privacy documentation
  • Coordinating logistical activities for study procedures in line with the study protocol
  • Processing lab samples
  • Performing data entry quality checks and resolving queries to ensure data accuracy and completeness
  • Patient education
  • 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:

  • Bachelors 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
  • Fluency in English

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.

Please note we cannot offer sponsorship for these positions.

#LI-HCPN

#LI-CES

#LI-DNP

#LI-CT1

#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

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.


Required Experience:

IC


Employment Type : Full-Time
Experience: years
Vacancy: 1
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Clinical Research Coordinator York • London, England, UK

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