At a Glance
- Tasks: Monitor clinical sites and ensure compliance with study protocols in oncology research.
- Company: Join IQVIA, a leader in healthcare innovation and research.
- Benefits: Full-time role with travel opportunities and professional growth.
- Other info: Dynamic field-based role with a focus on collaboration and impact.
- Why this job: Make a difference in healthcare while gaining valuable experience in clinical research.
- Qualifications: Experience in oncology monitoring and knowledge of GCP guidelines required.
The predicted salary is between 35000 - 45000 € per year.
Manchester, 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 startup 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*
Clinical Research Associate in Manchester 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 Manchester-based team is dedicated to supporting your professional growth through comprehensive training and development opportunities, while our commitment to work-life balance ensures you can thrive both personally and professionally. Join us in our mission to create a healthier world, where your contributions truly make a difference.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate in Manchester
✨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 lead to job opportunities that aren’t even advertised.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to site monitoring and GCP. We recommend doing mock interviews with friends or mentors to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your passion for oncology studies during interviews. We want to see your enthusiasm for making a difference in patients' lives, so share any relevant experiences or projects that highlight 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 Clinical Research Associate in Manchester
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.
Showcase Your GCP Knowledge:Since Good Clinical Practice is key for this role, make sure to mention your understanding and experience with GCP and ICH guidelines. We love candidates who can demonstrate their expertise in these areas!
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 keen on joining our team!
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 challenges they face. Being able to discuss recent advancements or common issues in this field will show that you're not just familiar with the role, but genuinely interested in it.
✨Master Good Clinical Practice (GCP)
Since GCP is a key part of the job, 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, as this will demonstrate your understanding and commitment to quality.
✨Show Off Your Communication Skills
As a Clinical Research Associate, you'll need to liaise with various stakeholders. Be ready to share examples of how you've effectively communicated with sites or team members in the past. Highlight any experience you have in training or managing expectations, as this will be crucial for the role.
✨Prepare for Site Monitoring Scenarios
Think through potential scenarios you might encounter during site visits. Be prepared to discuss how you would handle issues related to protocol adherence or recruitment challenges. This will showcase your problem-solving skills and readiness for the responsibilities of the position.
