Study Coordinator 3

A new & exciting opportunity has arisen for a Study Coordinator to join our team at our York Clinical Research Site.

The Study Coordinator 3 plays a key role in managing clinical trial data and supporting site compliance with regulatory and protocol standards. The role involves detailed data entry, documentation tracking, CRA visit preparation, and ensuring clinical and administrative readiness across all trial activities.

There may be a requirement to work across local Panthera sites as required from time to time.

Highly organised and data driven.

Skilled in accurate, timely data entry and query resolution

Evidence of experience working in a similar environment.

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.