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- Tasks: Support clinical trials and ensure smooth operations while collecting patient data.
- Company: Join IQVIA, a leader in clinical research with a focus on innovation.
- Benefits: Part-time role with flexible hours and the chance to make a real difference.
- Why this job: Be a vital part of groundbreaking medical research and improve patient outcomes.
- Qualifications: BS/BA in life sciences or relevant experience in a clinical setting.
- Other info: Great opportunity for career growth in a dynamic and supportive environment.
The predicted salary is between 24000 - 36000 £ per year.
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 clients.
- Good organizational skills with the ability to pay close attention to detail.
Clinical Research Coordinator -Wolverhampton, UK employer: IQVIA
Contact Detail:
IQVIA 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 industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by researching IQVIA and understanding their values and recent projects. Tailor your answers to show how your skills align with their mission. We want to see your passion for clinical research shine through!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or use online resources to refine your responses. Focus on articulating your experience in clinical settings and how it relates to the role of a Clinical Research Coordinator.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to engage with us directly.
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 any relevant experience in clinical settings and showcase your knowledge of clinical trials. 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 make you a great fit for our team. Keep it concise but engaging – we love a good story!
Show Off Your Skills: Don’t forget to mention your IT skills and attention to detail. We’re looking for someone who can handle data entry and maintain study protocols, so be sure to highlight your proficiency with MS Office and any other relevant tools.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re serious about joining our team at IQVIA!
How to prepare for a job interview at IQVIA
✨Know Your Clinical Trials
Make sure you brush up on your knowledge of clinical trials and the specific protocols related to the role. Familiarise yourself with common medical terminology and the processes involved in conducting a trial, as this will show your genuine interest and understanding of the field.
✨Showcase Your Organisational Skills
As a Clinical Research Coordinator, you'll need to juggle multiple tasks. Prepare examples from your past experiences where you've successfully managed projects or maintained attention to detail. This will demonstrate your ability to handle the responsibilities of the role effectively.
✨Prepare for Interpersonal Questions
Since this role involves working closely with investigators and volunteers, be ready to discuss how you build relationships and handle conflicts. Think of specific instances where you've successfully communicated or resolved issues, as this will highlight your interpersonal skills.
✨Familiarise Yourself with IT Tools
You’ll be using various software applications like MS Office and Electronic Data Capture systems. Brush up on these tools and be prepared to discuss your proficiency. If you have experience with data entry or quality checking, make sure to mention it during the interview.
