At a Glance
- Tasks: Support clinical studies and ensure participant safety while managing study documentation.
- Company: Join IQVIA, a leader in clinical research with a supportive team culture.
- Benefits: Flexible hours, remote work options, and valuable experience in the healthcare field.
- Other info: Short-term role with opportunities to grow your career in clinical research.
- Why this job: Make a real difference in clinical trials and advocate for patient well-being.
- 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? If so, join IQVIA as a Clinical Research Coordinator / Site Research Assistant to support a clinical study. This is a short‑term assignment of 6 months, working 13 hours per week, with the role 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.
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).
- Experience as a 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 Argentina
At IQVIA, we pride ourselves on being an exceptional employer, offering a supportive work culture that values collaboration and innovation in the field of clinical research. Our Blackburn location provides unique opportunities for professional growth, with flexible working arrangements that include both onsite and remote work, allowing you to balance your career with personal commitments. Join us to make a meaningful impact on clinical trials while enjoying a rewarding and dynamic work environment.
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 relevant events, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for those interviews by researching the company and the specific role. Familiarise yourself with their recent studies and projects. We want you to show them you’re genuinely interested and ready to contribute from day one!
✨Tip Number 3
Practice makes perfect! Get a friend or mentor to do mock interviews with you. This will help you articulate your experience and skills confidently. We believe in you, so let’s make sure you shine when it counts!
✨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 familiar names pop up in our system. Let’s get you that Clinical Research Coordinator role!
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 the 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’re looking for someone who can handle the technical side of things, so let us know how you’ve used these skills in past roles.
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 Argentina
✨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 capture systems. This will show that you're not just interested in the role but also understand what it entails.
✨Showcase Your Experience
Prepare to discuss your previous roles in clinical settings, especially any experience as a Research Nurse or Clinical Research Coordinator. Be ready to share specific examples of how you've handled participant concerns or maintained study documentation. This will help demonstrate your hands-on knowledge and problem-solving skills.
✨Highlight Your Interpersonal Skills
Since this role involves working closely with investigators and participants, be prepared to talk about how you build relationships. Share examples of how you've effectively communicated with colleagues or managed participant interactions. This will highlight your ability to advocate for patients and work well in a team.
✨Get Tech-Savvy
Brush up on your IT skills, especially with Microsoft Office applications. Be ready to discuss how you've used these tools in past roles, whether for data entry, managing inventory, or coordinating logistics. Showing that you're comfortable with technology will give you an edge in this data-driven role.
