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 focus on innovation.
- Benefits: Flexible hours, remote work options, and valuable experience in the healthcare field.
- 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.
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.
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
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 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
✨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 IQVIA and understanding their values and recent projects. Tailor your responses to show how your skills align with their mission. Practice common interview questions to boost your confidence!
✨Tip Number 3
Showcase your organisational skills! During interviews, share specific examples of how you've managed multiple tasks or projects in previous roles. This will demonstrate your ability to handle the responsibilities of a Clinical Research Coordinator.
✨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 our team.
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. Keep it concise but engaging!
Showcase Your Skills:Don’t forget to showcase your strong IT skills and attention to detail in your application. Mention specific software you’re proficient in, like Microsoft Office, and any relevant certifications or training you've completed.
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, so we can review it promptly!
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 capture systems. This will show that you're not just interested in the role but also understand what it entails.
✨Showcase Your Skills
Highlight your organisational skills and attention to detail during the interview. Prepare examples from your past experiences where you've successfully managed study documentation or coordinated logistics for clinical trials. This will help demonstrate your capability to handle the tasks required in this role.
✨Be a People Person
Since you'll be working closely with participants and colleagues, it's crucial to showcase your interpersonal skills. Think of instances where you've effectively communicated or resolved issues with team members or patients. This will illustrate your ability to build strong relationships, which is key in clinical research.
✨Prepare Questions
Have a few thoughtful questions ready to ask at the end of your interview. This could be about the study protocols, team dynamics, or how success is measured in the role. It shows your genuine interest in the position and helps you assess if the company is the right fit for you.
