Research Associate in Reading

Research Associate in Reading

Reading Full-Time 30000 - 40000 € / year (est.) No home office possible
High5

At a Glance

  • Tasks: Support Oncology studies by monitoring sites and ensuring compliance with regulations.
  • Company: Join a leading clinical research organisation in the heart of Reading.
  • Benefits: Full-time role with competitive salary and opportunities for travel.
  • Other info: Dynamic role with potential for career advancement in clinical research.
  • Why this job: Make a difference in cancer research while gaining valuable experience.
  • Qualifications: Life science degree or equivalent experience; independent monitoring skills required.

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

The Clinical Research Associate will support Oncology studies and cover sites across the UK.

  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
  • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
  • Escalate quality issues as appropriate.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
  • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
  • Collaborate and liaise with study team members for project execution support as appropriate.
  • Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
  • Life science degree educated or equivalent industry experience.
  • Flexibility to travel to sites as required.

Research Associate in Reading employer: High5

As a leading employer in the clinical research field, we offer our Research Associates a dynamic work environment in Reading, England, where innovation and collaboration thrive. Our commitment to employee growth is evident through comprehensive training programmes and opportunities for career advancement, all while fostering a supportive culture that values work-life balance and encourages professional development. Join us to make a meaningful impact in Oncology studies and be part of a team dedicated to excellence in clinical research.

High5

Contact Detail:

High5 Recruiting Team

StudySmarter Expert Advice🤫

We think this is how you could land Research Associate in Reading

Tip Number 1

Network like a pro! Reach out to professionals in the oncology field on LinkedIn or at local events. We can’t stress enough how valuable personal connections can be in landing that Research Associate role.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of Good Clinical Practice and site monitoring. We recommend practising common interview questions with a friend or even in front of the mirror to boost your confidence.

Tip Number 3

Showcase your flexibility and willingness to travel during interviews. As a Research Associate, you’ll need to visit various sites, so let’s highlight your adaptability and eagerness to get out there!

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.

We think you need these skills to ace Research Associate in Reading

Site Monitoring
Good Clinical Practice (GCP)
Subject Recruitment Planning
Protocol Administration
Communication Skills
Quality Evaluation
Regulatory Submissions Tracking

Some tips for your application 🫡

Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight any relevant experience in clinical research, especially in Oncology, and showcase your skills in site monitoring and project management.

Craft a Compelling Cover Letter:Your cover letter should tell us why you're the perfect fit for this position. Share specific examples of your past experiences that align with the job description, and don’t forget to express your enthusiasm for the role!

Showcase Your Communication Skills:Since the role involves liaising with various sites and team members, make sure to highlight your communication skills in your application. We want to see how you can effectively manage ongoing project expectations and issues.

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’re considered for the role. Plus, it’s super easy!

How to prepare for a job interview at High5

Know Your Oncology Stuff

Make sure you brush up on your knowledge of oncology studies and the specific protocols involved. Familiarise yourself with Good Clinical Practice (GCP) guidelines, as well as any recent developments in the field. This will show that you're not just interested in the role but also passionate about the subject matter.

Demonstrate Your Monitoring Skills

Be prepared to discuss your experience with site monitoring visits. Think of specific examples where you've successfully managed site selection, initiation, or close-out visits. Highlight how you’ve handled challenges in previous roles, especially regarding recruitment plans and maintaining communication with sites.

Showcase Your Organisational Skills

As a Research Associate, you'll need to manage multiple tasks simultaneously. Bring examples of how you've tracked regulatory submissions, monitored case report forms, or maintained documentation in the past. This will help illustrate your ability to keep everything organised and compliant.

Ask Insightful Questions

Prepare some thoughtful questions to ask during the interview. Inquire about the team dynamics, the specific challenges they face in their oncology studies, or how they measure success in this role. This shows that you're engaged and genuinely interested in contributing to their projects.