Clinical research associates & coordinators Work, Jobs in Willenhall, Wmd (with Salaries)

Clinical Research Coordinator -Wolverhampton, UK
IQVIA —Wolverhampton
- Part-time
- Microsoft Word
- Bachelor's degree
- Data entry
Band 6 Clinical Trials Research Nurse - Barberry
Birmingham and Solihull Mental Health NHS Foundation Trust —Birmingham
- £39,959 - £48,117 a year
- Full-time
8d
Data Manager (Surgical Data & Policy Hub) - College of Medicine and Health - 103809 - Grade 4
University of Birmingham —Birmingham
- £27,546 - £32,595 a year
- Full-time
- Word processing
- University
- Data entry
- Annual leave
- Sick pay
12h
Data Compliance Coordinator
Thermo Fisher Scientific —Birmingham
- Full-time
- Computer literacy
- English
- Quality control
6d
Data Manager - Department of Applied Health Sciences - 107770 - Grade 5
University of Birmingham —Birmingham
- £30,062 - £35,883 a year
- Part-time
- Computer literacy
- University
- Data entry
- Annual leave
- Sick pay
2d

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clinical research associates & coordinators jobs near willenhall, wmd

Clinical Research Coordinator -Wolverhampton, UK

IQVIA -
Wolverhampton

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Job details

Part-time

Qualifications

Microsoft Word
Healthcare research operations
Clinical research
Microsoft Office Suite
Bachelor's degree
Data entry
Recruiting
Organisational skills
Medical terminology

Full job description

Wolverhampton, United Kingdom | Part time | Field-based | R1557409

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.

This part-time (24 hours) role is to support a site in Wolverhampton in conducting a clinical trial.

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day to day responsibilities will include:

Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns
Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
Plan and coordinate logistical activity for study procedures according to the study protocol
Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
Correct custody of study drug according to site standard operating procedures
Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.

We are looking for candidates with the following skills and experience:

BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
Basic knowledge of medical terminology
Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
Good organizational skills with the ability to pay close attention to detail.

#LI-DNP

#LI-HCPN

#LI-CES

#LI-CT1

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.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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clinical research associates & coordinators jobs in willenhall, wmd

Clinical Research Coordinator -Wolverhampton, UK

Band 6 Clinical Trials Research Nurse - Barberry

Data Manager (Surgical Data & Policy Hub) - College of Medicine and Health - 103809 - Grade 4

Data Compliance Coordinator

Data Manager - Department of Applied Health Sciences - 107770 - Grade 5

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