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- Tasks: Support clinical trials, collect patient data, and ensure smooth operations.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Flexible part-time hours, gain valuable experience in the healthcare field.
- Why this job: Make a real difference in patient outcomes while developing your skills.
- Qualifications: Experience in clinical trials and strong IT skills required.
- Other info: Dynamic team environment with opportunities for growth and learning.
Research Assistant/Clinical Research Coordinator – London page is loaded## Research Assistant/Clinical Research Coordinator – Londonlocations: London, United Kingdomtime type: Part timeposted on: Posted Todayjob requisition id: R1508136This role is to support the site in **London** in conducting a clinical trial for **8** hours per week.As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.**Day to day responsibilities will include:*** Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator* Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns* Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents* Plan and coordinate logistical activity for study procedures according to the study protocol* Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues* Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness* Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol* Correct custody of study drug according to site standard operating procedures* Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.**We are looking for candidates with the following skills and experience:*** Two years of experience with clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules* Basic knowledge of medical terminology* Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word* Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client* Good organizational skills with the ability to pay close attention to detail. #LI-DNP#LI-CES#LI-HCPN#LI-CT1IQVIA 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. Learn more atIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. #J-18808-Ljbffr
Research Assistant/Clinical Research Coordinator - London employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Research Assistant/Clinical Research Coordinator - London
✨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 introductions. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for interviews by researching the company and the role. Familiarise yourself with their recent projects and values. We want to see that you’re genuinely interested and ready to contribute to the team!
✨Tip Number 3
Showcase your skills during interviews! Bring examples of your past experiences in clinical trials and how you’ve handled challenges. We love hearing about real-life situations where you made a difference.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always on the lookout for passionate candidates who are eager to join our mission.
We think you need these skills to ace Research Assistant/Clinical Research Coordinator - London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Research Assistant/Clinical Research Coordinator role. Highlight relevant experience, especially in clinical trials, and showcase your skills in data management and patient interaction.
Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for this position. Share your passion for clinical research and how your background aligns with our mission to improve patient outcomes.
Showcase Your Skills: Don’t forget to highlight your IT competence and organisational skills. Mention specific software you’re familiar with, like MS Office, and any experience you have with data entry or quality checking.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates regarding your application status.
How to prepare for a job interview at IQVIA LLC
✨Know Your Clinical Trials
Make sure you brush up on your knowledge of clinical trials and the specific protocols related to the role. Familiarise yourself with common medical terminology and the processes involved in conducting research. This will show that you're not just interested in the job, but that you understand the field.
✨Showcase Your Organisational Skills
Since this role involves a lot of administrative tasks, be prepared to discuss how you've successfully managed similar responsibilities in the past. Bring examples of how you've maintained attention to detail and ensured quality control in your previous roles.
✨Demonstrate Interpersonal Skills
This position requires excellent interpersonal skills, so think about times when you've effectively communicated with team members or clients. Be ready to share specific examples that highlight your ability to build relationships and advocate for volunteers.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about the clinical trials you'll be involved in, the team dynamics, or the company's approach to patient care. This shows your genuine interest in the role and helps you assess if it's the right fit for you.