Medical Monitor

Medical Monitor Psychiatry / reputed company 9-month contract Remote - some travel required to Princeton, NJ We are hiring a Medical Monitor with 6+ years of clinical drug development experience to support Phase 2 and Phase 3 Psychiatry and reputed company programs. This role combines medical monitoring, clinical data review, safety evaluation, and regulatory document support. You will work closely with Clinical Operations, Biometrics, Pharmacovigilance, Regulatory Affairs, and CRO partners across ongoing and upcoming studies. What Youll Work On Review safety and efficacy data from Phase 2 and Phase 3 studies Identify and assess emerging safety signals Support medical data review, data cleaning, and query reputed company Review SAEs and communicate with study sites as needed Contribute to protocols, CSRs, ISS/ISE documents, IBs, DSURs, and regulatory submissions Support protocol interpretation and study conduct during trial execution Partner with CROs on data review, reporting, and trial management activities Participate in Safety Review Team and cross-functional development meetings Background Required MD or equivalent physician qualification 6+ years of clinical development experience Psychiatry or reputed company experience required Experience supporting Phase 2 and/or Phase 3 studies Experience reviewing clinical safety and efficacy data Experience contributing to regulatory submission documents and clinical study reports Preferred CNS development experience FDA or global regulatory submission experience Experience in biotech or small-to-mid-sized reputed company environments ISS/ISE and safety document experience Apply tot his job Apply To this Job .