SSU sCRA - FSP

Parexel is currently seeking an experienced CRA  to join us in the UK. You will be assigned to one of our key sponsors in the region, focusing on SSU visits and activities for your assigned trials in the UK.

Whether you see your future path in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you.

Some specifics about this advertised role

• Dedicated to one client.

• Responsible for the selection and set-up of clinical studies up to site initiation.
• Performs Site Qualification Visits (on site or remote), completes SQV reports and inputs into site selection.
• Ensures that all study site documents under their responsibility are available, have been reviewed and uploaded to CTMS prior to site activation.
• Customizes plans with site team (eg. site recruitment plan, source data agreement)
• Acts as the main line of communication between the sponsor and the site team during study set-up.

• Trains, supports, and advises Investigators and site staff including pharmacy and other support departmental staff in study related assessments.
• Actively participates in local study team and set-up team meetings.
• Uploads time critical documents to eTMF

Here are a few requirements specific to this advertised role.

• Minimum of 3 years' experience independent monitoring.
• In depth experience of performing SSU activities
• Oncology trial experience is essential and only candidates with oncology trial experience can be considered.
• BSc in life sciences is preferred

We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long-term careers. In addition, you will have the opportunity to develop within your role and tackle further responsibilities or develop your skill set within other related departments of Parexel.

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.

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