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, remote work options, and valuable experience in a dynamic field.
- Other info: Short-term role with opportunities for growth and networking in the medical field.
- Why this job: Make a real difference in healthcare while gaining hands-on experience in clinical research.
- Qualifications: Degree in life sciences or relevant experience in a clinical setting required.
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
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 our team members can maintain a healthy work-life balance while making a meaningful impact in the field of clinical research.
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, 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 the company and the role. Familiarise yourself with IQVIA's projects and values, and think about how your skills as a Clinical Research Coordinator can contribute to their success. Confidence is key!
✨Tip Number 3
Showcase your skills! Bring along examples of your previous work, especially any experience related to clinical trials or patient advocacy. This will help you stand out and demonstrate your hands-on knowledge.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at IQVIA.
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 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 any experience with data management systems. We value strong organisational skills and attention to detail, so be sure to highlight these in your application. Let us know how you can contribute to maintaining a safe study environment!
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 keep track of your application status. Plus, we love seeing applications come directly from our site!
How to prepare for a job interview at IQVIA
✨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 in clinical trials, as well as IQVIA's approach to research. This will show your genuine interest and help you answer questions confidently.
✨Showcase Your Experience
Prepare to discuss your previous roles in clinical settings, especially any experience as a Clinical Research Coordinator or similar positions. Highlight specific examples where you’ve successfully managed study documentation or supported patient advocacy, as these are key aspects of the job.
✨Demonstrate Your IT Skills
Since strong IT skills are essential for this role, be ready to talk about your proficiency with Microsoft Office applications and any experience with Electronic Data Capture systems. You might even want to mention any relevant software you've used in past roles to illustrate your tech-savviness.
✨Ask Thoughtful Questions
Prepare some insightful questions to ask at the end of your interview. This could include inquiries about the team dynamics, the specific challenges of the study you'll be supporting, or how success is measured in this role. It shows you're engaged and thinking ahead about your potential contributions.
