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For Companies At a Glance
- Tasks: Lead site monitoring and ensure quality in clinical trials.
- Company: Join Parexel, a leader in clinical studies for top-selling drugs.
- Benefits: Enjoy remote work flexibility and opportunities for professional growth.
- Why this job: Make a real impact on patient well-being while developing your career.
- Qualifications: Experience in site management or CRA lead roles, especially in oncology.
- Other info: This role requires a commitment to learning and strong presentation skills.
The predicted salary is between 36000 - 60000 £ per year.
Parexel FSP has an exciting opportunity for an experienced Senior or Lead CRA to join as a Site and Monitoring Lead in the UK. As the SML, you will apply your knowledge of regulations, GCPs, and monitoring experience to ensure the quality of clinical trial execution at investigator sites and oversee CRO monitoring effectiveness. This is a site-facing role reporting to the FSP Manager.
Responsibilities include:
- Implementing oversight activities such as site risk analysis, site contacts, monitoring visit report review, sponsor oversight visits, and system/data checks.
- Creating study-specific oversight plans.
- Performing root cause analysis to identify issues and recommend actions.
- Building relationships with investigators and site staff.
- Providing support to less experienced investigator sites.
- Leading oversight and trend meetings.
Candidate Profile:
We seek professionals committed to patient well-being, demonstrating determination and courage. The role requires:
- Extensive Site Management or CRA Lead experience, especially in oncology trials.
- Clinical or Advanced degree preferred; BSc or BA essential.
- Strong presentation skills.
- Client-focused approach and professional interaction skills.
- Flexibility and willingness to learn.
- Ability to prioritize tasks and meet project deadlines independently.
Site and Monitoring Lead - FSP - Remote - UK employer: TN United Kingdom
Contact Detail:
TN United Kingdom Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Site and Monitoring Lead - FSP - Remote - UK
✨Tip Number 1
Familiarise yourself with the latest regulations and guidelines related to clinical trials, especially GCPs. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high standards in clinical research.
✨Tip Number 2
Network with professionals in the clinical research field, particularly those who have experience in oncology trials. Attend relevant webinars or local meetups to build connections that could lead to referrals or insider information about the role.
✨Tip Number 3
Prepare to discuss specific examples of how you've successfully managed site oversight activities in previous roles. Highlight your ability to perform root cause analysis and implement effective solutions, as these are key responsibilities for the Site and Monitoring Lead.
✨Tip Number 4
Showcase your strong presentation skills by preparing a mock presentation on a relevant topic in clinical trials. This will not only boost your confidence but also provide a tangible example of your communication abilities during the interview process.
We think you need these skills to ace Site and Monitoring Lead - FSP - Remote - UK
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of the Site and Monitoring Lead position. Familiarise yourself with the key requirements such as site management experience and knowledge of GCPs.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical trials, particularly in oncology. Emphasise your leadership roles and any specific achievements that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for patient well-being and your commitment to quality in clinical trials. Use specific examples from your past experiences to demonstrate how you meet the qualifications outlined by Parexel.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for spelling and grammatical errors, and ensure that all information is clear and concise. A polished application reflects your attention to detail.
How to prepare for a job interview at TN United Kingdom
✨Know Your Regulations
Familiarise yourself with the relevant regulations and Good Clinical Practices (GCPs) before the interview. Being able to discuss these confidently will demonstrate your expertise and commitment to quality in clinical trial execution.
✨Showcase Your Experience
Prepare specific examples from your previous roles that highlight your site management or CRA lead experience, particularly in oncology trials. This will help illustrate your capability to handle the responsibilities of the Site and Monitoring Lead position.
✨Emphasise Relationship Building
Since the role involves building relationships with investigators and site staff, be ready to discuss how you've successfully fostered professional relationships in the past. This will show your client-focused approach and interpersonal skills.
✨Demonstrate Problem-Solving Skills
Be prepared to talk about a time when you performed root cause analysis to identify issues in a project. Highlight the actions you recommended and the outcomes, as this will showcase your analytical thinking and ability to improve processes.
