Offer summary

Qualifications:

Substantial Site Management or CRA Lead experience in clinical research, particularly in oncology trials., Clinical or Advanced degree preferred, with a BSc or BA essential., Excellent presentation skills and a client-focused approach., Strong analytical skills with the ability to prioritize multiple tasks..

Key responsibilities:

Implement various types of oversight encounters and activities, including site risk analysis and monitoring visit report review.

Build relationships with investigators and site staff, providing support to less experienced sites.

Lead oversight and trend meetings to ensure effective monitoring and compliance.

Perform root cause analysis to identify issues and suggest actions to study management and CRO partners.

Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Parexel FSP has an upcoming exciting opportunity for an experienced Senior or Lead CRA to join one of our key sponsors in the UK as a Site and Monitoring Lead.

As the SML you will apply knowledge of regulations and GCPs as well as experience in monitoring to safeguard the quality of clinical trial execution at investigator sites and ensure the client’s oversight of CRO monitoring effectiveness.

This is a site-facing position that reports to the FSP Manager.

Some specifics about this advertised role

Implements various types of oversight encounters and activities as applicable including
- Site risk analysis
- Site contacts
- Monitoring visit report review
- Sponsor Oversight Visits
- System/data spot checks
Creating study specific oversight plans
Perform root cause analysis to identify issues and suggest actions to study Management and CRO partners.
Build relationships with investigators and site staff
Provide investigator sites less experienced in research
Leading oversight and trend meetings

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well-being of many patients.

You’ll be an influential member of the wider team.

What we are looking for in this role

For every role, we look for professionals who have the determination and courage always to put patient well-being first.

That to us is working with heart.

Here are a few requirements specific to this advertised role.

Substantial Site Management or CRA Lead experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. Specifically within oncology trials.
Clinical or Advanced degree preferred, BSc or BA essential
Excellent presentation skills.
Client focused approach to work.
Ability to interact professionally within a client organization.
Flexible attitude with respect to work assignments and new learning.
Ability to prioritize multiple tasks, and achieve project timelines; utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise.

Required profile