At Zave, we our proud that we are able to contribute to advancing medical treatments to enable more people to be healthier, live longer and enjoy a better quality of life.
Our people are the cornerstone to our success and are the difference in us being able to deliver our projects successfully with validity of data and integrity. Our company culture is supportive and energetic and is built around;
Compassion
Innovation
Flexibility
Hard work
Accuracy
You could be a good fit for Zave if you are…
Hard working, detail oriented and compassionate.
An excellent communicator. We need people that can create a great rapport with trial participants, investigators and clinic staff as well as the many and varied stakeholders that they would be dealing with (patients, clinic doctors, clinic technical staff, clinic admin staff, study sponsors and monitors as well as third party service providers).
A combination of being assertive yet obliging to be able to effectively coordinate and manage trials and influence key stakeholders.
A problem solver, lateral thinker and pay great attention to detail. We need our people to have the ability to follow protocols and guidelines, but they also need to be able to navigate through any issues that may arise throughout the trial process.
Team orientated but also able to work effectively independently.
Experienced and confident in patient-based environments.
Typical roles within the Zave team
Clinical Project Manager
Reporting to the Managing Directors, this role provides overall project management for single/multi-site trials from feasibility stage to close-out; provide leadership for teams (both ZAVE and clinic staff); are engaged to conduct trials at the site level; as well as involvement with coordination of trials at the site level.
Clinical Trial Coordinator
This role reports to a Clinical Project Manager and oversees day to day clinical trial coordination operations at the site level for investigators; liaises with clinic staff and third party vendors to ensure patient visits and data is collected in compliance with ICH GCP and the study protocol.
Clinical Trials Assistant/Research Technician
Reporting directly to the Clinical Trial Coordinator; this role is involved in clinical examinations and collection of study data; as well as assisting with data entry and trial administrative tasks at the request of the trial coordinator.
Clinical Trial Coordinator Internship
10-12 week internship consisting of 6-8 week Introduction to Clinical Trials training component (remote learning) and 4 week on-site practical component (1-2 days per week); Theory component consists of 8 training modules reviewed over 6-8 weeks with 1-2 weekly zoom calls scheduled with a Clinical Project Manager to discuss the content and ask questions; Practical on-site component involves accompanying a Clinical Project Manager on site, reviewing trial materials and observing planning for clinical trial patient visits and conduct of patient visits.