At a Glance
- Tasks: Monitor oncology studies and ensure compliance with clinical protocols.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Gain valuable experience, travel opportunities, and contribute to meaningful health outcomes.
- Other info: Dynamic role with opportunities for growth and learning in a supportive environment.
- Why this job: Make a real impact in the fight against cancer while advancing your career.
- Qualifications: Experience in oncology monitoring and knowledge of GCP guidelines required.
The predicted salary is between 30000 - 40000 € per year.
IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. The Clinical Research Associate will support Oncology studies and cover sites across the UK.
Responsibilities:
- 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. May support start-up phase.
- 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.
Requirements:
- Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
- In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Life science degree educated or equivalent industry experience.
- Flexibility to travel to sites as required.
Research Associate – Oncology in Peacehaven employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and continuous learning. As a Research Associate in Oncology, you will have the opportunity to make a meaningful impact on patient outcomes while benefiting from comprehensive training and career development programmes. Our commitment to employee growth, coupled with our global presence and innovative approach to clinical research, makes IQVIA a rewarding place to advance your career in the heart of the UK.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate – Oncology in Peacehaven
✨Tip Number 1
Network like a pro! Reach out to professionals in the oncology field on LinkedIn or at industry 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 GCP and ICH knowledge. We recommend practising common interview questions related to site monitoring and study management, so you can showcase your expertise confidently.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values. At StudySmarter, we believe in making an impact, so look for roles that resonate with your passion for improving patient outcomes.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the position. We always appreciate a candidate who takes the initiative to stay engaged.
We think you need these skills to ace Research Associate – Oncology in Peacehaven
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight your experience in Oncology and any relevant monitoring visits you've conducted. We want to see how your background aligns with our mission!
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 you can contribute to our team. Keep it engaging and personal – we love a good story!
Showcase Your GCP Knowledge:Since Good Clinical Practice is key in this role, make sure to mention your understanding of GCP and ICH guidelines. We’re looking for candidates who can demonstrate their commitment to quality and compliance.
Apply Through Our Website:Don’t forget to apply 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 – just a few clicks and you’re done!
How to prepare for a job interview at IQVIA
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of oncology and the specific studies you'll be working on. Familiarise yourself with the latest trends and challenges in the field, as this will show your passion and commitment to the role.
✨Master Good Clinical Practice (GCP)
Since GCP is a big part of the job, ensure you understand its principles inside out. Be ready to discuss how you've applied these guidelines in previous roles, as this will demonstrate your expertise and reliability.
✨Prepare for Site Monitoring Scenarios
Think about potential site monitoring scenarios you might face and how you'd handle them. This could include recruitment challenges or quality issues. Practising your responses will help you feel more confident during the interview.
✨Show Your Communication Skills
As a Clinical Research Associate, you'll need to communicate effectively with various stakeholders. Prepare examples of how you've successfully managed communication in past projects, highlighting your ability to build relationships and resolve issues.
