We are looking for a Medical Monitor to join our team and play a key role in driving the success of our clinical trials. This position offers the opportunity to provide medical, scientific, and strategic leadership across all stages of clinical development – from protocol design through study execution to final reporting.
In this role, you will act as the medical expert within our organisation, overseeing participant safety, reviewing and interpreting clinical data, and ensuring compliance with GCP and regulatory standards. You will also collaborate closely with cross-functional teams and external stakeholders, contributing medical insight to study design & project planning.
Responsibilities:
* Provide medical management and oversight for clinical trials.
* Contribute medical expertise to study reports, regulatory documents, and manuscripts.
* Manage and assess safety issues in clinical trials, working closely with study teams.
* Participate in business development activities, including proposals and sponsor meetings as required.
* Collaborate with cross-functional teams across all study phases, including feasibility, protocol design, medical information management, and educational initiatives.
* Review and edit medical documents to ensure accuracy and compliance.
Qualifications/Needs:
* Qualified medical doctor (MD) with active medical license
* Background in pharmaceutical or CRO clinical research is advantageous
* Proven experience working on clinical trials
You’ll provide the medical insight and leadership that ensures patient safety and drives the success of our clinical trials. We’re seeking dedicated professionals who want to advance the future of medicine while upholding the highest standards of care. At our core, we value diversity, inclusion, and equal opportunity—and we invite you to join us in shaping innovation and transforming healthcare worldwide.