Site and Monitoring Lead - FSP - Remote - UK

TN United Kingdom; London; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading company in clinical research seeks a Site and Monitoring Lead to ensure quality execution of clinical trials. The role involves oversight activities, building relationships with site staff, and supporting less experienced sites. Ideal candidates have extensive CRA Lead experience, strong presentation skills, and a commitment to patient well-being.

Qualifications

• Extensive Site Management or CRA Lead experience, especially in oncology trials.

Responsibilities

• Implementing oversight activities such as site risk analysis and monitoring visit report review.
• Creating study-specific oversight plans.
• Performing root cause analysis to identify issues.

Skills

Presentation Skills

Client-focused Approach

Flexibility

Task Prioritization

Education

BSc or BA

Clinical or Advanced Degree

Job description

Site and Monitoring Lead - FSP - Remote - UK, London

Client: Parexel

Location: London, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: f18c775f386b

Job Views: 3

Posted: 17.05.2025

Expiry Date: 01.07.2025

Job Description:

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.

About Parexel:

Parexel supports clinical studies across various therapeutic areas, partnering with a broad client base. We have contributed to trials of many top-selling drugs and niche developments critical to patient well-being.

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.