At a Glance
- Tasks: Monitor clinical sites and support Oncology studies across the UK.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Gain valuable experience, make an impact, and enjoy continuous learning.
- Other info: Flexible travel required; great opportunity for career growth in a dynamic environment.
- Why this job: Be part of a mission to create a healthier world through innovative medical treatments.
- Qualifications: Experience in Oncology monitoring and knowledge of GCP and ICH guidelines.
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. Apply today and forge a career with greater purpose, make an impact and never stop learning!
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.
*Please note - this role is not eligible for visa sponsorship.*
Research Associate in Kiveton Park 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, you will have the opportunity to make a meaningful impact in the field of Oncology while benefiting from comprehensive training and career development programmes. Our commitment to employee growth, coupled with our mission to improve global health outcomes, makes IQVIA a truly rewarding place to advance your career.
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate in Kiveton Park
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those working at IQVIA. A friendly chat can open doors and give you insights that might just land you an interview.
✨Tip Number 2
Prepare for the interview by brushing up on your knowledge of Good Clinical Practice (GCP) and Oncology studies. We want you to shine when discussing your experience and how it aligns with the role!
✨Tip Number 3
Showcase your flexibility and willingness to travel. Mention specific instances where you've adapted to changing project needs or gone the extra mile to ensure success. It’s all about demonstrating your commitment!
✨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 take the initiative to connect directly with us.
We think you need these skills to ace Research Associate in Kiveton Park
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight your experience in Oncology studies and any relevant skills that match the job description. We want to see how you can make an impact!
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 background aligns with our mission at IQVIA. Keep it engaging and personal.
Showcase Your GCP Knowledge:Since Good Clinical Practice (GCP) is crucial for this role, make sure to mention your understanding and experience with GCP and ICH guidelines. We love candidates who know their stuff!
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 shows you’re serious about joining our team!
How to prepare for a job interview at IQVIA
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of Oncology studies and the specific protocols involved. Being able to discuss recent advancements or challenges in the field will show that you're genuinely interested and informed.
✨Master Good Clinical Practice (GCP)
Since GCP is a big part of the role, ensure you can talk confidently about its principles and how they apply to site monitoring. Prepare examples from your past experiences where you adhered to these guidelines.
✨Showcase Your Communication Skills
As a Clinical Research Associate, you'll need to liaise with various stakeholders. Be ready to demonstrate your ability to communicate effectively, whether it’s through examples of managing site expectations or resolving issues.
✨Prepare for Travel Questions
Since the role requires flexibility to travel, think about how you manage your time and logistics when visiting multiple sites. Be prepared to discuss your approach to balancing travel with study management.
