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For Companies At a Glance
- Tasks: Support clinical trials by managing data and ensuring participant safety.
- Company: Join IQVIA, a leader in clinical research and innovation.
- Benefits: Flexible part-time hours with opportunities for growth in the healthcare field.
- Why this job: Be part of groundbreaking research that impacts lives while gaining valuable experience.
- Qualifications: BS/BA in life sciences or relevant experience in a clinical setting required.
- Other info: Work 15 hours per week in Halifax, West Yorkshire.
The predicted salary is between 24000 - 36000 £ per year.
Job Description
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 role is to support a site in Halifax, West Yorkshire in conducting a clinical trial for 15 hours per week.
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.
Clinical Research Coordinator employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Coordinator
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in clinical research. This will not only help you understand the role better but also demonstrate your commitment to staying updated in this fast-paced field.
✨Tip Number 2
Network with professionals already working in clinical research. Attend relevant workshops or webinars, and connect with them on platforms like LinkedIn. This can provide you with insider knowledge about the role and potentially lead to referrals.
✨Tip Number 3
Prepare for potential interview questions by practising responses that highlight your organisational skills and attention to detail. Think of specific examples from your past experiences that showcase these abilities in action.
✨Tip Number 4
Research IQVIA as a company and their specific projects. Understanding their mission and values will allow you to tailor your conversations during interviews, showing that you are genuinely interested in being part of their team.
We think you need these skills to ace Clinical Research Coordinator
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research or related fields. Emphasise any roles where you've supported clinical trials, managed data, or worked with medical professionals.
Craft a Strong Cover Letter: Write a cover letter that specifically addresses the responsibilities and skills mentioned in the job description. Explain why you're passionate about clinical research and how your background makes you a great fit for the role.
Highlight Relevant Skills: In your application, clearly outline your knowledge of clinical trials, medical terminology, and IT skills. Mention any experience with data entry, quality checking, or patient interaction to demonstrate your suitability for the position.
Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in a clinical research environment.
How to prepare for a job interview at IQVIA
✨Know Your Clinical Research Basics
Make sure you brush up on your knowledge of clinical trials and the specific protocols related to the role. Being able to discuss these topics confidently will show that you're well-prepared and understand the industry.
✨Highlight Relevant Experience
Be ready to share examples from your past work that demonstrate your skills in a clinical environment. Whether it's coordinating studies or managing patient data, specific anecdotes can make a strong impression.
✨Showcase Your IT Skills
Since the role requires proficiency in MS Office and other software, be prepared to discuss your experience with these tools. You might even want to mention any specific projects where you used these applications effectively.
✨Demonstrate Interpersonal Skills
As a Clinical Research Coordinator, you'll need to work closely with various stakeholders. Be ready to talk about how you've built effective working relationships in the past and how you handle communication with team members and participants.
