At a Glance
- Tasks: Support clinical studies and ensure participant safety while managing essential study documentation.
- Company: Join IQVIA, a leader in clinical research with a focus on innovation.
- Benefits: Flexible hours, remote work options, and valuable experience in the healthcare industry.
- Other info: Short-term role with opportunities for growth in a dynamic environment.
- Why this job: Make a real difference in patient care 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.
As a pivotal member of the site team, you will be involved in a variety of clinical and administrative tasks to support investigators in ensuring the smooth running of clinical trials.
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.
- 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 in London 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 healthcare sector. With a flexible work schedule that includes both onsite and remote work, we ensure a healthy work-life balance while empowering our team members to make a meaningful impact on patient outcomes.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Coordinator - Blackburn in London
✨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! During interviews, be ready to discuss specific examples of your experience in clinical trials, data management, and participant care. Use the STAR method (Situation, Task, Action, Result) to structure your answers.
✨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 genuinely interested in joining IQVIA and being part of their mission to improve patient outcomes.
We think you need these skills to ace Clinical Research Coordinator - Blackburn in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Coordinator role. Highlight relevant experience and skills that match the job description, like your knowledge of clinical trials and any previous roles in a medical setting.
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 background makes you a great fit for the team. Keep it concise but impactful!
Showcase Your Skills:Don’t forget to showcase your IT skills and attention to detail in your application. Mention specific software you’re proficient in, like Microsoft Office, and any experience with data entry or managing study documentation.
Apply Through Our Website:We encourage you to apply through our website for the best chance of success. It’s straightforward and ensures your application goes directly to us, making it easier for us to review your credentials!
How to prepare for a job interview at IQVIA
✨Know Your Stuff
Make sure you brush up on clinical research basics and the specific responsibilities of a Clinical Research Coordinator. Familiarise yourself with common protocols, case report forms, and data management systems. This will show that you're not just interested in the role but also understand what it entails.
✨Show Your Interpersonal Skills
Since this role involves working closely with participants and colleagues, be ready to demonstrate your excellent interpersonal skills. Think of examples where you've built strong relationships or resolved conflicts. This will help you stand out as someone who can effectively advocate for study participants.
✨Be Organised and Detail-Oriented
Highlight your organisational skills during the interview. You might want to share specific instances where your attention to detail made a difference in a project. This is crucial in clinical research, so showing that you can manage multiple tasks without missing a beat will impress the interviewers.
✨Ask Smart Questions
Prepare thoughtful questions about the study and the team you'll be working with. This shows your genuine interest in the position and helps you gauge if the company culture aligns with your values. Questions about how they ensure participant safety or how they handle data accuracy can be particularly insightful.
