Study Coordinator

We are looking for an experienced and highly organised Study Coordinator to join our team at our at our Preston Clinical Research Site.

This is a key site based role and we are looking for an individual to join the team, taking study ownership, keeping studies on track and making sure the detail is right. You’ll work closely with clinical teams, monitors, vendors and site colleagues to support the smooth delivery of clinical trials!

If you have experience working in clinical research and are confident managing study documentation, data and competing priorities, we’d love to hear from you.

You’ll be someone who is organised, detail-focused and comfortable taking responsibility for multiple study activities at once.

Previous experience in clinical research or a similar regulated environment

Experience coordinating clinical studies and maintaining study documentation

Strong data-entry skills with excellent attention to accuracy and deadlines

A good understanding of clinical trial documentation and regulatory requirements

Strong communication skills and the confidence to work with colleagues, monitors and external partners

The ability to prioritise effectively and keep studies moving forward

We are an equal opportunity employer and consider all qualified applicants equally without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, veteran status or disability status.

Panthera is an independent Site Management Organisation helping pharmaceutical and contract research organisations find the right patient, for the right trial, at the right time. The Panthera team is run by a world-class team of experts with more than a hundred years of clinical research experience.

We put the patient at the heart of everything we do to ensure the best experience and environment for volunteers and participants. Accelerating clinical breakthrough for our customers, our patients, and for future generations.