At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research regulations.
- Company: Leading clinical research organisation focused on innovative healthcare solutions.
- Benefits: Competitive salary, flexible hours, and opportunities for professional growth.
- Other info: Collaborative environment with strong support for career advancement.
- Why this job: Join a dynamic team and contribute to groundbreaking research that impacts lives.
- 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.
Research Associate in Failsworth employer: Iqvia Uk's Site Management
As a leading organisation in clinical research, we pride ourselves on fostering a collaborative and supportive work environment for our Research Associates. Located in the heart of the UK, we offer competitive benefits, continuous professional development opportunities, and a culture that values innovation and integrity. Join us to make a meaningful impact in the field of clinical trials while advancing your career in a dynamic and rewarding setting.
Contact Details:
Iqvia Uk's Site Management Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Research Associate in Failsworth
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the hunt for a Research Associate role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on GCP and ICH guidelines. Make sure you can discuss how you've applied these in your previous roles. We want to see you shine and show that you’re the perfect fit for the responsibilities outlined in the job description!
✨Tip Number 3
Don’t just wait for job alerts! Actively search for opportunities on our website and apply directly. Tailor your application to highlight your monitoring experience and your ability to manage site relationships effectively.
✨Tip Number 4
Follow up after interviews with a thank-you email. It’s a great way to reiterate your interest in the position and remind them of your relevant skills. Plus, it shows you’re proactive and keen on the role!
We think you need these skills to ace Research Associate in Failsworth
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Research Associate role. Highlight your relevant experience, especially any independent on-site monitoring 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 clinical research and how your background fits with our mission at StudySmarter. Keep it engaging and personal.
Showcase Your Knowledge:Demonstrate your understanding of GCP and ICH guidelines in your application. We love candidates who can speak the language of clinical research and show they’re up-to-date with industry standards.
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 the StudySmarter 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 experience, especially any interventional studies you've worked on. Highlight how you managed site visits, tracked regulatory submissions, and resolved data queries. This will help the interviewer 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 establish and maintain effective working relationships. Share examples of how you’ve communicated project expectations and resolved issues in the past to demonstrate your interpersonal skills.
✨Be Ready for Scenario Questions
Expect scenario-based questions where you might need to evaluate a hypothetical situation related to site management or protocol adherence. Think through how you would handle potential quality issues or recruitment challenges, as this will showcase your problem-solving abilities.
