Medical Monitor
Responsibilities
- Provide scientific and medical input across clinical development programs, collaborating with internal teams and external partners.
- Review and interpret clinical trial safety and efficacy data to inform program decisions and regulatory documentation.
- Contribute to authoring, reviewing, and finalizing key clinical and regulatory documents for protocols, clinical study reports, and submissions.
- Support oversight and interaction with CROs and vendors regarding clinical data, reports, and regulatory deliverables.
Requirements
- A physician with a minimum of 6 years of drug development experience.
- Experience within Psychiatry or Neurology.
- Demonstrated ability to analyze and interpret clinical trial data, including safety and efficacy outcomes.
- Prominent track record preparing and reviewing regulatory and clinical documents for clinical trial protocols and submissions.
About the Role
We are seeking a dedicated professional to support clinical development efforts for Phase 2 and Phase 3 studies. Our team values scientific and medical expertise to drive program success and ensure data integrity throughout the clinical trial process.
About SSI People
With over 26 years of industry experience, SSi People has built its reputation and expertise on putting people first. Everything we do works toward delivering exceptional experience for our consultants, our clients, and our internal team. Through a genuine commitment to people in everything we do. We have developed refined processes and a stellar internal team to deliver talent quickly. More importantly, we focus on building long-term relationships, not transactions. Putting people first is just what we do well.