At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research regulations.
- Company: Leading oncology research organisation focused on innovative treatments.
- Benefits: Competitive salary, flexible hours, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on career development.
- Why this job: Join a mission-driven team making a difference in cancer research.
- Qualifications: 1 year of monitoring experience and knowledge of GCP and ICH guidelines.
The predicted salary is between 30000 - 40000 £ per year.
Responsibilities
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- 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.
- 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
- Requires at least 1 year of independent on-site monitoring experience of interventional studies in the UK.
- Good knowledge and skill in applying applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- Good therapeutic and protocol knowledge as provided in company training.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Oncology Research Associate: Site Monitoring & Study Delivery in Leeds employer: Iqvia Uk's Site Management
As an Oncology Research Associate, you will thrive in a dynamic and supportive work environment that prioritises employee growth and development. Our company fosters a culture of collaboration and innovation, offering comprehensive training and mentorship opportunities to enhance your skills in clinical research. Located in the heart of the UK, we provide a unique chance to contribute to impactful studies while enjoying a balanced work-life atmosphere.
Contact Details:
Iqvia Uk's Site Management Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Oncology Research Associate: Site Monitoring & Study Delivery in Leeds
✨Tip Number 1
Network like a pro! Reach out to professionals in the oncology research field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on GCP and ICH guidelines. We recommend having specific examples ready that showcase your monitoring experience and how you’ve tackled challenges in past studies.
✨Tip Number 3
Don’t just apply and wait! Follow up with the hiring manager after submitting your application through our website. A quick email expressing your enthusiasm can set you apart from other candidates.
✨Tip Number 4
Showcase your adaptability! In your conversations, highlight how you’ve successfully managed site relationships and adapted recruitment plans. We want to see how you can drive project success!
We think you need these skills to ace Oncology Research Associate: Site Monitoring & Study Delivery in Leeds
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Oncology Research Associate role. Highlight your relevant experience in site monitoring and your understanding of GCP and ICH guidelines. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about oncology research and how your background makes you a great fit for our team. Keep it engaging and personal – we love to see your personality come through!
Showcase Your Experience:When detailing your experience, focus on specific examples that demonstrate your ability to manage studies and maintain quality standards. We’re keen to see how you've tackled challenges in previous roles, so don’t hold back!
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 shows you’re proactive and keen to join our team!
How to prepare for a job interview at Iqvia Uk's Site Management
✨Know Your GCP and ICH Guidelines
Make sure you brush up on Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines before the interview. Being able to discuss these regulations confidently will show that you understand the core of the role and can apply them effectively in your work.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your previous monitoring experiences, especially those related to interventional studies. Highlight how you managed site visits, tracked regulatory submissions, and resolved data queries. This will help the interviewers see your practical skills in action.
✨Show Your Communication Skills
Since the role involves liaising with study sites and team members, be ready to discuss how you've established effective communication lines in past roles. Share instances where you successfully managed project expectations or resolved issues through clear communication.
✨Be Ready for Scenario Questions
Expect scenario-based questions that test your problem-solving abilities. Think about potential challenges you might face in site monitoring and how you would address them. This will demonstrate your critical thinking and adaptability in real-world situations.
