$300,000–$390,000/yr
US
Unlimited PTO
- Serves as the medical monitor for clinical trials and assists in resolving major issues that may affect their assigned studies.
- Partners with the Clinical Scientist, Data Manager, Pharmacovigilance Scientist, and other members of the study team to conduct the clinical studies.
- Provides expert opinion and review for creation of key study documents, including clinical study protocols, safety and medical monitoring plans, charters, and informed consent forms.