At a Glance
- Tasks: Support clinical studies and ensure participant safety while managing essential documentation.
- Company: Join IQVIA, a leader in clinical research with a collaborative environment.
- 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 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 promote a healthy work-life balance, making it an ideal environment for those passionate about advancing healthcare. Join us to make a meaningful impact while enjoying the benefits of a dynamic team dedicated to excellence in clinical trials.
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 specific role. Familiarise yourself with their recent projects and values, so you can show how you fit into their team and contribute to their goals.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or family to get comfortable with common questions. This will help you articulate your experience and skills confidently when it counts.
✨Tip Number 4
Don't forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can sometimes give you an edge. Plus, it’s super easy to keep track of your applications!
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 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. Don’t forget to mention your interpersonal skills and attention to detail!
Showcase Your IT Skills:Since strong IT skills are essential for this role, make sure to mention your proficiency in Microsoft Office applications. If you have experience with Electronic Data Capture systems, definitely include that too!
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 directly!
How to prepare for a job interview at IQVIA Argentina
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trials and the specific responsibilities of a Clinical Research Coordinator. Familiarise yourself with common protocols, consent forms, and the latest trends in clinical research. This will show that you're not just interested in the role but also understand its intricacies.
✨Showcase Your Skills
Prepare to discuss your relevant experience in detail. Whether it's your time as a Research Nurse or your familiarity with EDC systems, be ready to provide examples of how you've successfully managed similar tasks. Highlight your IT skills and how they can benefit the team.
✨Be a People Person
Interpersonal skills are key in this role, so think about how you can demonstrate your ability to build relationships. Prepare anecdotes that showcase your communication skills and how you've effectively worked with colleagues, participants, and study monitors in the past.
✨Ask Smart Questions
At the end of the interview, don’t forget to ask insightful questions. Inquire about the team dynamics, the specific studies you'll be involved in, or how success is measured in this role. This shows your genuine interest and helps you assess if the company is the right fit for you.
