At a Glance
- Tasks: Coordinate and manage clinical studies from start to finish in a dynamic environment.
- Company: Join ICON, a leader in clinical research partnering with top pharmaceutical companies.
- Benefits: Enjoy a competitive salary, flexible remote work options, and a supportive workplace culture.
- Why this job: Make a real impact in healthcare while working in an innovative and inclusive team.
- Qualifications: A science degree or equivalent experience in clinical trials is required.
- Other info: This role is office-based in Luton, with a mix of remote work.
The predicted salary is between 36000 - 60000 £ per year.
Here at the ICON Global Strategic Solutions team, we are looking to add a further employee to our growing group of experienced Senior Clinical Study Administrators in Luton. We are considering candidates with relevant clinical research experience and a solid understanding of clinical research.
You will be partnering with a well-known global pharmaceutical company with a strong portfolio in a variety of clinical trials. You will have an opportunity to work in a solid partnership and an environment driven by innovation and continuous improvement. This program is for you if you are looking for an environment where people feel they belong and are empowered to reach their full potential, perform at their best and make a valued contribution to saving lives.
Responsibilities
- The Senior Clinical Study Administrator assists in the coordination and administration of clinical study activities within the study start-up team and the Local Study Team, ensuring the quality and timeliness of study deliverables regarding scope, budget, and quality standards.
- Reporting to the Clinical Administration Manager, you will coordinate and administer clinical studies from start-up through execution and close-out.
- It is desirable that candidates have similar clinical trial experience within the pharmaceutical industry.
- You will be responsible for collecting, assisting in the preparation, reviewing, and tracking of documents for the clinical trial application process.
- You will contribute to the production and maintenance of study documents, ensuring compliance with templates and version control.
- Additionally, you will support document translation when required.
- Working closely with the Project Leader and CRA teams, you will manage multiple clinical studies simultaneously.
- The role requires comfort working in a fast-paced environment.
Qualifications
- Science degree or equivalent.
- Permanent full-time contract with ICON, embedded with one client.
- Office-based in the Luton area (England): minimum 3 days per week in the office and 2 days remote work.
- Competitive salary depending on skills and experience, plus company benefits.
At ICON, inclusion and belonging are fundamental to our culture and values. We are committed to providing an inclusive and accessible environment for all candidates. ICON promotes a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
Snr Clinical Study Administrator - Luton employer: Symphony Health
Contact Detail:
Symphony Health Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Snr Clinical Study Administrator - Luton
✨Tip Number 1
Familiarise yourself with the specific clinical trials that the global pharmaceutical company is involved in. Understanding their portfolio will not only help you during interviews but also demonstrate your genuine interest in the role and the company.
✨Tip Number 2
Network with current or former employees of ICON or similar companies. Engaging with them on platforms like LinkedIn can provide you with insider knowledge about the company culture and expectations, which can be invaluable during your application process.
✨Tip Number 3
Brush up on your knowledge of clinical trial regulations and compliance standards. Being well-versed in these areas will not only prepare you for potential interview questions but also show that you are proactive and ready to contribute from day one.
✨Tip Number 4
Prepare to discuss your experience managing multiple projects simultaneously. The ability to juggle various clinical studies is crucial for this role, so having concrete examples ready will help you stand out as a candidate who can thrive in a fast-paced environment.
We think you need these skills to ace Snr Clinical Study Administrator - Luton
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the responsibilities and qualifications required for the Senior Clinical Study Administrator position. Tailor your application to highlight relevant experience in clinical research.
Highlight Relevant Experience: In your CV and cover letter, emphasise any previous roles in clinical trial administration or related fields. Provide specific examples of how you've contributed to study start-up processes or document management.
Showcase Your Skills: Make sure to mention skills that are crucial for this role, such as attention to detail, ability to manage multiple projects, and familiarity with compliance standards in clinical research. Use concrete examples to demonstrate these skills.
Craft a Compelling Cover Letter: Write a personalised cover letter that connects your background to the values and mission of ICON. Express your enthusiasm for the role and how you can contribute to their commitment to innovation and saving lives.
How to prepare for a job interview at Symphony Health
✨Showcase Your Clinical Research Knowledge
Make sure to brush up on your clinical research knowledge before the interview. Be prepared to discuss your previous experiences in clinical trials and how they relate to the role of a Senior Clinical Study Administrator.
✨Demonstrate Organisational Skills
Since the role involves managing multiple studies simultaneously, highlight your organisational skills. Share examples of how you've successfully coordinated projects or managed timelines in past roles.
✨Familiarise Yourself with Compliance Standards
Understanding compliance and quality standards is crucial in this position. Be ready to discuss how you ensure adherence to these standards in your work, especially regarding document management and version control.
✨Emphasise Team Collaboration
This role requires working closely with various teams. Prepare to talk about your experience collaborating with others, particularly in fast-paced environments, and how you contribute to a positive team dynamic.