Clinical research coordinator york Work, Jobs in Hambleton, Nyk (with Salaries)

Clinical Research Coordinator - York
IQVIA —York
- Part-time
- Microsoft Word
- Microsoft Excel
- Microsoft Access
8d
Care Coordinator
Leeds and York Partnership NHS Foundation Trust —Leeds
- £39,959 - £48,117 a year
- Full-time
- Hybrid work
- Organisational skills
- Care plans
- Annual leave
- Employee discount
6d
Support Service Secretary
Leeds and York Partnership NHS Foundation Trust —Leeds
- £25,760 - £27,476 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Customer service
- Annual leave
- Employee discount
6d

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Clinical Research Coordinator - York
IQVIA —York
Must have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site.
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Clinical Research Coordinator - York

IQVIA -
York

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Job details

Part-time
8 days ago

Qualifications

Microsoft Word
Microsoft Excel
Microsoft Access
Microsoft Outlook
Clinical research
English
Microsoft Office
Bachelor's degree
Organisational skills
IT
Medical terminology
Communication skills

Full 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:

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
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 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.

Apply Now

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Clinical Research Coordinator - York

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