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 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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Top Skills
What We Do
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.
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