Description
Allucent is hiring an Associate Medical Director to independently support the medical, clinical, and safety integrity of oncology clinical trials. The role includes medical monitoring, protocol interpretation, medical monitoring plans, SAE/SUSAR review, MedDRA and WHO coding, clinical document review, data safety and dose-escalation committee participation, urgent medical support, risk management, and client and site engagement. The position requires an MD, oncology experience, at least three years of relevant professional experience, GxP knowledge, regulatory and communication skills, and proficiency with Word, Excel, and PowerPoint. The role is remote, with hybrid work depending on location and requiring two office days per week for employees within reasonable distance of a global office.

