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- Tasks: Coordinate clinical studies, report adverse events, and manage data entry.
- Company: Join a dynamic team focused on advancing medical research.
- Benefits: Gain hands-on experience in clinical research with potential for growth.
- Why this job: Perfect for those passionate about healthcare and making a difference.
- Qualifications: Must have 1-2 years of clinical research experience and EDC knowledge.
- Other info: Immediate interviews available for qualified candidates!
The predicted salary is between 28800 - 43200 £ per year.
This is an exciting opportunity with candidates to start and interview as soon as possible!
The Clinical Study Coordinator must have minimum 1/2 years\’ clinical research experience as they need an individual who can work independently as well as part of a team. Day to day responsibilities will involve a reporting adverse events, data entry, administrative tasks and query resolution.
Requirements:
EDC experience (medidata rave)
Clinical Research Coordinator employer: Actalent
Contact Detail:
Actalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Coordinator
✨Tip Number 1
Make sure to highlight your clinical research experience during the interview. Be prepared to discuss specific projects you've worked on and how you contributed to their success.
✨Tip Number 2
Familiarize yourself with Medidata Rave if you haven't already. Being able to demonstrate your knowledge of this EDC system can set you apart from other candidates.
✨Tip Number 3
Showcase your ability to work both independently and as part of a team. Prepare examples that illustrate your adaptability in different working environments.
✨Tip Number 4
Be ready to discuss how you handle adverse events and data entry tasks. Having concrete examples will help demonstrate your competence in these critical areas.
We think you need these skills to ace Clinical Research Coordinator
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasize your clinical research experience in your application. Detail your previous roles, responsibilities, and any specific projects you've worked on that relate to the position of Clinical Research Coordinator.
Showcase EDC Proficiency: Since EDC experience is a requirement, clearly outline your familiarity with Medidata Rave or any other electronic data capture systems you have used. Provide examples of how you've utilized these tools in past roles.
Detail Your Teamwork Skills: The job requires someone who can work both independently and as part of a team. Include examples in your application that demonstrate your ability to collaborate effectively with others while also managing tasks on your own.
Proofread Your Application: Before submitting, carefully proofread your application for any errors or typos. A well-written application reflects your attention to detail, which is crucial in clinical research.
How to prepare for a job interview at Actalent
✨Show Your Clinical Research Experience
Be prepared to discuss your previous clinical research roles in detail. Highlight specific projects you've worked on, focusing on your responsibilities and the outcomes achieved.
✨Demonstrate Teamwork and Independence
Since the role requires both independent work and collaboration, share examples of how you've successfully navigated both situations in past positions. This will show your versatility.
✨Familiarize Yourself with EDC Systems
Make sure you understand the basics of Electronic Data Capture (EDC) systems, particularly Medidata Rave. If you have experience with it, be ready to discuss how you've used it in your previous roles.
✨Prepare for Administrative Task Questions
Expect questions about your organizational skills and how you handle administrative tasks. Think of examples where you efficiently managed data entry or resolved queries to demonstrate your capabilities.
