At a Glance
- Tasks: Support clinical trials by managing data and ensuring participant safety.
- Company: Join IQVIA, a leader in the clinical research industry.
- Benefits: Enjoy flexible part-time hours and gain valuable experience in healthcare.
- Other info: This role is based in Halifax, West Yorkshire, for 15 hours per week.
- Why this job: Be part of groundbreaking research that impacts lives while working in a supportive team environment.
- Qualifications: A degree in life sciences or relevant experience in a clinical setting is required.
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 Leeds 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.
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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.
Clinical Research Coordinator in Leeds employer: IQVIA
At IQVIA, we pride ourselves on being an industry leader in clinical research, offering a supportive and collaborative work environment in Halifax, West Yorkshire. Our part-time Clinical Research Coordinator role not only provides meaningful work that contributes to advancing healthcare but also offers opportunities for professional growth and development within a dynamic team. With a strong focus on employee well-being and a commitment to maintaining a safe study environment, we ensure that our staff feel valued and empowered in their roles.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Coordinator in Leeds
✨Tip Number 1
Network with professionals in the clinical research field. Attend local events or join online forums related to clinical trials and research. This can help you gain insights into the role and potentially connect you with someone who can refer you to us.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in clinical research. Understanding current practices will not only boost your confidence but also demonstrate your commitment to the field during interviews.
✨Tip Number 3
Prepare for potential interview questions by reviewing common scenarios faced by Clinical Research Coordinators. Think about how you would handle specific challenges, as this will show your problem-solving skills and readiness for the role.
✨Tip Number 4
Showcase your IT skills by being proficient in MS Office applications, especially Excel. Consider creating a sample data entry project or a mock study protocol to demonstrate your capabilities during the interview process.
We think you need these skills to ace Clinical Research Coordinator in Leeds
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 Compelling Cover Letter:Write a cover letter that showcases your passion for clinical research and your understanding of the role. Mention specific skills that align with the job description, such as your knowledge of clinical trials and your organisational abilities.
Highlight Relevant Skills:In your application, clearly outline your IT competence, especially with MS Office applications. Provide examples of how you've used these skills in previous roles to manage data or support research activities.
Showcase Interpersonal Skills:Since the role requires excellent interpersonal skills, include examples of how you've successfully collaborated with teams or built relationships in past positions. This will demonstrate your ability to work effectively within a clinical 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 prepared and understand the industry.
✨Highlight Relevant Experience
Be ready to talk about your previous roles in clinical environments or any relevant work experience. Use specific examples to demonstrate how your background aligns with the responsibilities of a Clinical Research Coordinator.
✨Showcase Your IT Skills
Since the role requires strong IT competence, be prepared to discuss your experience with MS Office applications and any other relevant software. You might even want to mention any specific projects where you used these skills effectively.
✨Demonstrate Interpersonal Skills
As a Clinical Research Coordinator, you'll need to work closely with various stakeholders. Be ready to share examples of how you've built effective working relationships in the past, showcasing your excellent interpersonal skills.
