Study Start Up Associate - IVDR experience required
Study Start Up Associate - IVDR experience required

Study Start Up Associate - IVDR experience required

Full-Time 30000 - 40000 £ / year (est.) Home office possible
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At a Glance

  • Tasks: Assist in preparing and submitting regulatory documents for clinical studies.
  • Company: Join ICON plc, a leading healthcare intelligence and clinical research organisation.
  • Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
  • Other info: Inclusive culture with opportunities for personal and professional growth.
  • Why this job: Make a real impact in clinical development while working remotely.
  • Qualifications: Bachelor's degree in life sciences and IVDR experience required.

The predicted salary is between 30000 - 40000 £ per year.

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a Study Start Up Associate at ICON, embedded within a growing program, you will be responsible for collecting, preparing, reviewing, approving, processing and tracking regulatory and site level critical documents required for study site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable country regulations/guidelines and the principles of ICH/GCP.

What You Will Do:

Your role will involve delivering site start-up and activation work to a high standard, working closely with your team and stakeholders. Key responsibilities include:

  • Assisting in the preparation and submission of regulatory documents, such as clinical trial applications and ethics committee submissions.
  • Coordinating with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation.
  • Maintaining accurate and up-to-date records of regulatory submissions and approvals.
  • Supporting study teams in the development of study documents, including protocols, informed consent forms, and investigator brochures.
  • Participating in study start-up meetings and providing input on regulatory requirements and timelines.

Your Profile:

You will bring relevant site start-up and activation experience, along with the following qualifications and skills:

  • Bachelor's degree in life sciences or a related field.
  • Must have IVDR experience.
  • Ideally you will have IVD and IDE submissions experience.
  • Previous experience in clinical research or regulatory affairs preferred, but not required.
  • Strong attention to detail and organizational skills.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.
  • Ability to work independently and manage multiple tasks simultaneously in a fast-paced environment.
  • Willingness to travel as required (approximately 5%).

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family. Our benefits examples include:

  • Various annual leave entitlements.
  • A range of health insurance offerings to suit you and your family’s needs.
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
  • Life assurance.
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Study Start Up Associate - IVDR experience required employer: IRE

At ICON plc, we pride ourselves on being a world-leading healthcare intelligence and clinical research organisation that champions innovation and excellence. Our inclusive work culture fosters collaboration and personal growth, offering competitive benefits such as flexible working arrangements, comprehensive health insurance, and a global employee assistance programme. Join us in shaping the future of clinical development while enjoying a supportive environment that values your contributions and well-being.
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Contact Detail:

IRE Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Study Start Up Associate - IVDR experience required

✨Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field, especially those with IVDR experience. A friendly chat can lead to insider info about job openings or even a referral.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of regulatory documents and site activation processes. We want you to shine when discussing your experience and how it aligns with ICON's mission.

✨Tip Number 3

Don’t underestimate the power of follow-ups! After an 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, you’ll find all the latest roles that match your skills and interests.

We think you need these skills to ace Study Start Up Associate - IVDR experience required

IVDR experience
Clinical Trial Applications
Ethics Committee Submissions
Regulatory Submissions
Attention to Detail
Organisational Skills
Communication Skills
Interpersonal Skills
Collaboration
Ability to Work Independently
Time Management
Knowledge of ICH/GCP Principles
Experience in Clinical Research
Experience in Regulatory Affairs

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Study Start Up Associate role. Highlight your IVDR experience and any relevant skills that match the job description. We want to see how your background fits with 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 research and how your experience aligns with our mission at ICON. Keep it concise but impactful – we love a good story!

Show Off Your Attention to Detail: In this role, attention to detail is key. Make sure your application is free from typos and errors. We appreciate candidates who take the time to present their best selves, so double-check everything before hitting send!

Apply Through Our Website: We encourage you to apply directly through our careers site. It’s the best way to ensure your application gets into the right hands. Plus, you’ll find all the info you need about the role and our awesome benefits there!

How to prepare for a job interview at IRE

✨Know Your IVDR Inside Out

Make sure you brush up on your In Vitro Diagnostic Regulation (IVDR) knowledge. Be prepared to discuss how your experience aligns with the requirements of the role, and think of specific examples where you've successfully navigated regulatory submissions.

✨Showcase Your Attention to Detail

As a Study Start Up Associate, attention to detail is crucial. During the interview, highlight instances where your meticulous nature has led to successful outcomes in previous roles. Bring along any relevant documents or examples that demonstrate your organisational skills.

✨Communicate Effectively

Since you'll be coordinating with various stakeholders, practice articulating your thoughts clearly. Prepare to discuss how you've collaborated with cross-functional teams in the past, and be ready to answer questions about how you handle communication challenges.

✨Prepare for Scenario Questions

Expect scenario-based questions that assess your problem-solving abilities. Think about potential challenges you might face in the role and how you would address them. This will show your proactive approach and readiness to tackle the responsibilities of the position.

Study Start Up Associate - IVDR experience required
IRE

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