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- Tasks: Support clinical trials with high-level administration and ensure compliance with protocols.
- Company: Re:Cognition Health, a leader in cognitive impairment clinical services.
- Benefits: Competitive salary, 25 days annual leave, private health insurance, and continuous professional development.
- Other info: Exciting growth opportunities in a supportive work environment.
- Why this job: Join a dynamic team making a real impact in clinical research and patient care.
- Qualifications: Experience in clinical administration and knowledge of ICH GCP protocols.
The predicted salary is between 28500 - 28500 £ per year.
About the Company: Re: Cognition Health is a leading provider of clinical services specializing in cognitive impairment. We deliver expert clinical care to private patients and are one of the foremost providers of clinical trials in the world and deliver award winning medico-legal services. We value people who are dedicated, hardworking and looking to contribute to the growth of the business at an exciting time.
The Senior Clinical Trials Administrator will play a pivotal role in the day to day running of the Clinical Trials conducted at the site, closely working with the Study Coordinator(s). The role involves high level administration responsibilities for the clinical trials, to support the Study Coordinator(s) and supporting with the scheduling of patient visits, whilst ensuring compliance with the International Conference on Harmonisation guidelines for Good Clinical Practice (ICH GCP) and specific protocols as designated by the trial Sponsors and Clinical Research Organisations.
Clinical Trials Administrator Responsibilities:
- Assist the Study Coordination team, with the clinical trials taking place at the site, by providing high level administrative support, ensuring that the studies are conducted and documented according to the study protocol and ICH GCP.
- Serve as a key member of the site team with the goal to contribute towards efficient management of clinical trials, support the Study Coordinator(s) with study setup, delivery and close out.
- Manage the essential documentation for the portfolio of trials at the site, ensuring consistency with documents held electronically, and compliance with ICH GCP Essential documents.
- Maintain adequate records and ensure all relevant information is accurately documented in the study participant’s files.
- Perform data entry in accord with sponsor or trial requirements and systems and ensure data queries are resolved promptly.
- Assist with the administration of all study related documents in site files/patient binders.
Salary: £28,500
Role: Permanent, Full time, On Site
Essential Criteria:
- Previous administration experience in a clinical setting
- Previous experience in managing protocols (ICH-GCP qualified)
- IT Proficiency (Microsoft Office package)
- Good verbal and written communication skills
Desirable:
- Clinical trials experience in an NHS, academic or commercial setting
- Experience of managing essential documents for clinical trials according to ICH GCP
Benefits:
- Continuous professional development
- 25 Days Annual Leave + Bank Holidays, increasing to 30
- Private Health Insurance
- Life insurance
- Employee Assistance Program
- Pension Scheme
- Perkbox
- Free Mortgage Advisor Scheme
- Electric Vehicle Scheme
If you think that you are suitable for this Senior Clinical Trials Administrator role, please apply now!
Senior Clinical Trials Administrator - Re:Cognition Health Birmingham employer: Re:cognition Health Clinics
Contact Detail:
Re:cognition Health Clinics Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Trials Administrator - Re:Cognition Health Birmingham
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical trials field, especially those who might know someone at Re:Cognition Health. A friendly chat can sometimes lead to opportunities that aren’t even advertised.
✨Tip Number 2
Prepare for the interview by brushing up on ICH GCP guidelines and the specific protocols relevant to the role. Show us you’re not just a fit on paper but also ready to hit the ground running!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After your interview, drop a quick thank-you email to express your appreciation and reiterate your enthusiasm for the role. It keeps you fresh in their minds.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at Re:Cognition Health.
We think you need these skills to ace Senior Clinical Trials Administrator - Re:Cognition Health Birmingham
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Clinical Trials Administrator role. Highlight your previous administration experience in a clinical setting and any relevant qualifications, especially those related to ICH GCP. We want to see how your skills match 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 trials and how you can contribute to our team at Re:Cognition Health. Keep it concise but engaging – we love a good story!
Show Off Your IT Skills: Since IT proficiency is essential, make sure to mention your experience with Microsoft Office and any other relevant software. If you've used specific tools for data entry or document management, let us know – we’re keen to see your tech-savvy side!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep everything organised and ensures your application gets the attention it deserves. Plus, it’s super easy!
How to prepare for a job interview at Re:cognition Health Clinics
✨Know Your Stuff
Make sure you brush up on your knowledge of ICH GCP guidelines and the specific protocols relevant to clinical trials. Being able to discuss these in detail will show that you're not just familiar with the basics, but that you truly understand the intricacies of the role.
✨Showcase Your Experience
Prepare examples from your previous administration roles in a clinical setting. Highlight how you've managed protocols and documentation, as well as any challenges you've faced and how you overcame them. This will demonstrate your hands-on experience and problem-solving skills.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to clinical trials. Think about how you would handle scheduling conflicts or data discrepancies. Practising these scenarios can help you articulate your thought process clearly during the interview.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions about the company’s approach to clinical trials or their future projects. This shows your genuine interest in the role and helps you gauge if the company aligns with your career goals.