At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research regulations.
- Company: Leading oncology research organisation dedicated to advancing cancer treatments.
- Benefits: Competitive salary, flexible hours, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation and career development.
- Why this job: Join a mission-driven team making a real difference in cancer research.
- Qualifications: 1 year of on-site monitoring experience and knowledge of GCP/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 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
✨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 personal connections can lead to job opportunities that aren’t even advertised.
✨Tip Number 2
Prepare for interviews by practising common questions related to site monitoring and study delivery. We recommend role-playing with a friend or using online resources to get comfortable discussing your experience with GCP and ICH guidelines.
✨Tip Number 3
Showcase your skills! Create a portfolio or a presentation that highlights your previous monitoring experiences and successes. We love seeing candidates who can demonstrate their impact on study quality and subject recruitment.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we often have exclusive roles listed there that you won’t find anywhere else.
We think you need these skills to ace Oncology Research Associate: Site Monitoring & Study Delivery
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Oncology Research Associate role. Highlight your relevant experience, especially any site monitoring or clinical research work you've done. We want to see how your skills align with our needs!
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 the team. Keep it engaging and personal – we love to see your personality!
Showcase Your Regulatory Knowledge:Since this role involves adhering to GCP and ICH guidelines, make sure to mention your understanding of these regulations in your application. We’re looking for someone who can navigate the complexities of clinical research with ease!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us you’re keen on joining the StudySmarter family!
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 your interview. Being able to discuss these regulations confidently will show that you understand the core of the role and can apply them effectively in site monitoring.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your previous experience where you successfully conducted site monitoring visits. Highlight how you managed recruitment plans, tracked regulatory submissions, and resolved data queries. This will help the interviewers see your practical knowledge in action.
✨Showcase Your Communication Skills
Since the role involves establishing regular lines of communication with sites, be ready to discuss how you've effectively communicated with team members and clients in the past. Share instances where you managed expectations or resolved issues through clear communication.
✨Prepare Questions About the Role
Think of insightful questions to ask about the company's approach to study delivery and site management. This not only shows your interest in the position but also gives you a chance to assess if the company aligns with your career goals and values.
