Medical Monitoring Associate

The Medical Monitoring Associate provides medical consultation to therapeutic sites under the Medical Director's guidance.

After completing your training, you will be well placed to provide answers to queries from physicians and nurses. Working according to relevant Standard Operating Procedures, the study protocol and Safety and Medical Management Plans, you will be responsible for the review of medical and lab reports. Given your medical expertise, investigator site staff including study nurses will seek clarification from you on patient inclusion / exclusion criteria. Tracking protocol violations, escalating issues to the Medical Director and compiling information as requested all form part of this varied and demanding role.

To be a successful candidate in this position it is preferred to bring previous experience within clinical research.

Given the client-focused and fast-paced nature of our work, we are looking for a pro-active individual with a strong eye for detail.

Ideally you are an undergraduate with a healthcare or a life sciences related background and understanding of medical terminology.

Certified or licensed scientific / health care professionals or those with first experience in clinical research are preferred, but this is not required.

Familiarity with medical terminology, strong organisational abilities, and a proven ability to use MS Office are skills essential to success in this role. Fluency in English is required.

LI-AB1

LI-DNP

LI-Onsite