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- Tasks: Support clinical trials and ensure smooth operations while collecting patient data.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Part-time hours with flexible scheduling and opportunities for professional growth.
- Why this job: Make a real difference in patient outcomes while gaining valuable experience.
- Qualifications: BS/BA in life sciences or relevant experience in a clinical setting.
- Other info: Dynamic team environment with a focus on innovation and impact.
The predicted salary is between 13 - 16 £ per hour.
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 clients
- Good organizational skills with the ability to pay close attention to detail.
Clinical Research Coordinator -Wolverhampton, UK employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Coordinator -Wolverhampton, UK
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend local events, and join relevant online groups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and understanding their clinical trials. Be ready to discuss how your skills align with their needs. Practise common interview questions and think of examples from your experience that showcase your abilities.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a thank-you email expressing your appreciation for the opportunity. It shows your enthusiasm and keeps you fresh in their minds.
✨Tip Number 4
Apply through our website for the best chance at landing that Clinical Research Coordinator role. We love seeing candidates who take the initiative to engage directly with us. Plus, it makes tracking your application easier!
We think you need these skills to ace Clinical Research Coordinator -Wolverhampton, UK
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Coordinator role. Highlight relevant experience in clinical settings and any specific skills that match the job description. We want to see how your background aligns with what we’re looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical research and how your skills can contribute to our team. Keep it concise but engaging – we love a good story!
Showcase Your Attention to Detail: In clinical research, attention to detail is crucial. Make sure your application is free from typos and errors. We appreciate candidates who take the time to present their best work, so double-check everything before hitting send!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, you’ll get to explore more about our company while you’re at it!
How to prepare for a job interview at IQVIA LLC
✨Know Your Clinical Trials
Make sure you brush up on your knowledge of clinical trials and the specific protocols related to the role. Being able to discuss how you would maintain a safe study environment or handle patient data will show that you're not just familiar with the basics, but that you understand the nuances of the job.
✨Showcase Your Interpersonal Skills
As a Clinical Research Coordinator, you'll need to interact with various stakeholders, including patients and investigators. Prepare examples of how you've successfully built relationships in previous roles. This will demonstrate your ability to advocate for volunteers and address their concerns effectively.
✨Get Familiar with IT Tools
Since strong IT competence is key for this role, make sure you're comfortable with MS Office applications, especially Excel and Access. You might be asked about your experience with data entry or managing study documents, so having specific examples ready will help you stand out.
✨Attention to Detail is Key
In clinical research, accuracy is everything. Be prepared to discuss how you've ensured quality control in past projects. Whether it's through meticulous data checking or maintaining up-to-date study protocols, showing that you have a keen eye for detail will resonate well with interviewers.
