Your mission

As Clinical Development Medical Monitor, you will provide medical oversight across Ferrer’s clinical studies, helping to ensure participant safety, data quality, and medically sound decision‑making throughout the conduct of clinical trials.

Your essential role will be to provide medical expertise on all medically relevant matters, including medical consultation, medical data review, and review of essential study documents. You will also support the early identification of safety concerns across the clinical studies managed and overseen by Ferrer’s Clinical Development Department, ensuring a consistent and standardized approach to medical monitoring activities.

As a key medical partner to internal teams and external providers, especially CROs, you will help ensure that medical monitoring activities are conducted in line with protocol, regulatory requirements, and ethical standards. In addition, you will contribute to fostering strong medical ...