At a Glance
- Tasks: Monitor clinical sites and ensure adherence to protocols for Oncology studies.
- Company: Join IQVIA, a leader in healthcare innovation and research.
- Benefits: Gain valuable experience, competitive salary, and opportunities for travel.
- Other info: Dynamic role with opportunities for growth and learning in a supportive environment.
- Why this job: Make a real difference in healthcare while developing your career in clinical research.
- Qualifications: Life science degree or equivalent experience; knowledge of GCP and ICH guidelines.
The predicted salary is between 35000 - 45000 € per year.
Oxfordshire, United Kingdom | Full time | Field-based | R1514135
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.
Qualifications
- 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.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Clinical Research Associate employer: IQVIA Argentina
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the field of clinical research. Our commitment to employee growth is evident through comprehensive training programmes and opportunities to work on impactful Oncology studies across the UK, all while contributing to our mission of creating a healthier world. With a focus on integrity and professionalism, we ensure that our team members are supported and empowered to excel in their roles.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. We can’t stress enough how personal connections can open doors to opportunities that aren’t even advertised.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. We recommend practising common interview questions, especially those related to site monitoring and GCP. Show them you’re not just a candidate, but the right fit for their mission!
✨Tip Number 3
Follow up after interviews! A simple thank-you email can set you apart from other candidates. We believe it shows your enthusiasm and professionalism, which are key traits for a Clinical Research Associate.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Research Associate role. Highlight your experience in Oncology studies and any relevant skills that match the job description. We want to see how you fit into 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 your background aligns with our goals at StudySmarter. Keep it engaging and personal.
Be Honest and Clear:Remember, honesty is key! Ensure all the information you provide is truthful and complete. We appreciate transparency, and it helps us get to know the real you. No need for embellishments!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets to us quickly and efficiently. Plus, you’ll find all the details you need about the role there!
How to prepare for a job interview at IQVIA Argentina
✨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 not just familiar with the basics, but genuinely interested in the area.
✨Master Good Clinical Practice (GCP)
Since GCP is a big part of the role, ensure you can confidently explain its principles and how they apply to site monitoring. Prepare examples from your past experiences where you adhered to these guidelines, as this will demonstrate your commitment to quality and compliance.
✨Show Off Your Communication Skills
As a Clinical Research Associate, you'll need to liaise with various stakeholders. Practice articulating how you've effectively communicated with sites in the past, especially when managing expectations or resolving issues. Clear communication is key!
✨Be Ready to Discuss Problem-Solving
Think of specific instances where you've encountered challenges during site monitoring and how you overcame them. This could involve recruitment issues or regulatory hurdles. Highlighting your problem-solving skills will show that you're proactive and resourceful.
