At a Glance
- Tasks: Support clinical research studies and ensure participant safety while maintaining study documentation.
- Company: Join IQVIA, an industry leader in clinical research.
- Benefits: Flexible hours with a mix of onsite and remote work.
- Other info: Gain valuable experience in a dynamic environment with potential for growth.
- Why this job: Make a difference in healthcare by advocating for study participants.
- Qualifications: BS/BA in life sciences or relevant experience in a clinical setting.
The predicted salary is between 30000 - 40000 € 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 is currently looking for a Clinical Research Coordinator/Site Research Assistant to support a clinical study. This is a short-term study assignment (6 months), working 13 hours per week, supporting a site in Blackburn. The role is one day onsite and half a day remote each week.
Key Responsibilities
- Support clinical research studies and maintain a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.
- Safeguard the well-being of study participants, act as a patient advocate, and address participant concerns.
- Maintain up-to-date study documentation, including study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other essential records.
- Plan and coordinate logistical activities for study procedures in line with the study protocol.
- Perform clinical study set-up and preparation, including labeling specimen collection tubes and containers, managing inventory of required supplies, and setting up or troubleshooting study equipment.
- Assist with data entry, data quality checks, and query resolution to ensure protocol compliance and data accuracy.
- Support study enrollment activities, including recruiting, screening, and orienting participants according to the study protocol.
- Ensure correct custody and handling of study medication in accordance with site standard operating procedures.
- Coordinate with study monitors on study-related issues and respond effectively to monitor-initiated queries.
- Perform and document patient vital signs.
Required Skills And Experience
- BS/BA in life sciences or equivalent education and/or relevant work experience in a clinical or medical setting (e.g., Clinical Research Coordinator, Research Nurse, Medical Assistant, or similar role).
- Ideally an experienced Research Nurse or a highly experienced Clinical Research Coordinator/Site Research Assistant.
- Strong knowledge of clinical trials, including departmental, protocol-specific, and study-specific operating procedures, consent forms, and study schedules.
- Strong IT skills, with proficiency in MS Windows and Microsoft Office applications (Access, Outlook, Excel, Word).
- Excellent interpersonal skills with the ability to build and maintain effective working relationships with colleagues, managers, and clients.
- Strong organizational skills with close attention to detail.
Clinical Research Coordinator - Blackburn employer: IQVIA Laboratories
At IQVIA, we pride ourselves on being an industry leader in clinical research, offering a supportive and collaborative work environment in Blackburn. Our commitment to employee growth is evident through our comprehensive training programmes and opportunities for advancement within the company. With a flexible work schedule that includes both onsite and remote work, we ensure a healthy work-life balance while fostering a culture of innovation and excellence.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Coordinator - Blackburn
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and the role. Understand IQVIA's mission and values, and think about how your skills as a Clinical Research Coordinator align with their needs. This will help you stand out during the interview.
✨Tip Number 3
Practice your responses to common interview questions. Focus on your experience in clinical trials and how you've handled challenges in previous roles. Being well-prepared will boost your confidence and help you articulate your value.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you're serious about joining the team at IQVIA and ready to make an impact in clinical research.
We think you need these skills to ace Clinical Research Coordinator - Blackburn
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Coordinator role. Highlight relevant experience, especially 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 you can contribute to our team. Keep it concise but engaging – we love a good story that connects your experience to the role.
Show Off Your Skills:Don’t forget to highlight your IT skills and attention to detail. Mention your proficiency in Microsoft Office and any experience with data entry or managing study documentation. We’re keen on candidates who can keep everything organised and accurate!
Apply Through Our Website:We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to track your application status. Plus, it shows us you’re serious about joining our team!
How to prepare for a job interview at IQVIA Laboratories
✨Know Your Stuff
Make sure you brush up on clinical research basics and the specific protocols related to the role. Familiarise yourself with common terms and processes, as well as the responsibilities outlined in the job description. This will show that you're genuinely interested and prepared.
✨Showcase Your Experience
Be ready to discuss your previous roles in clinical settings. Highlight any relevant experience you have as a Clinical Research Coordinator or similar positions. Use specific examples to demonstrate how you've successfully managed studies or supported patient care.
✨Ask Smart Questions
Prepare thoughtful questions about the study you'll be supporting and the team dynamics. This not only shows your enthusiasm but also helps you gauge if the company culture aligns with your values. Think about asking about their approach to participant advocacy or how they handle data accuracy.
✨Demonstrate Your Interpersonal Skills
Since this role involves working closely with participants and colleagues, be sure to convey your strong interpersonal skills during the interview. Share examples of how you've built relationships in past roles and how you handle conflicts or challenges with grace.
