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 Royal Tunbridge Wells 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 Royal Tunbridge Wells
✨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 creating a cheat sheet of key points to discuss, so you can show off your knowledge and confidence when it counts!
✨Tip Number 3
Don’t just apply and wait! Follow up with a friendly email to express your enthusiasm for the role. It shows initiative and keeps you on their radar—trust us, it makes a difference!
✨Tip Number 4
Check out our website for the latest job openings. We’re always looking for passionate individuals like you, and applying directly through us can give you an edge in the hiring process!
We think you need these skills to ace Oncology Research Associate: Site Monitoring & Study Delivery in Royal Tunbridge Wells
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:In your application, be sure to showcase any independent on-site monitoring experience you've had. We’re particularly interested in how you've managed studies and ensured compliance with regulations. Specific examples will make your application stand out!
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’s super easy – just follow the prompts and submit your materials!
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 site monitoring.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your previous experience where you successfully conducted site monitoring visits. Highlight how you managed issues, tracked progress, and ensured compliance with protocols. This will help the interviewer see your practical skills in action.
✨Show Your Communication Skills
Since the role involves liaising with various stakeholders, be ready to discuss how you establish and maintain effective working relationships. Share examples of how you've communicated with sites to manage expectations and resolve issues, as this is crucial for success in the position.
✨Be Ready to Discuss Recruitment Strategies
Think about how you would adapt and drive a subject recruitment plan. Be prepared to share your ideas on enhancing predictability in recruitment and how you’ve tackled similar challenges in the past. This shows your proactive approach and understanding of project needs.
