Medical Monitor

About This Role

This role is for an experienced Medical Monitor Contractor to support a dynamic, global clinical development program within a leading pharmaceutical company. The position involves contributing medical and scientific expertise to the oversight of interventional clinical trials, focusing on data review, patient safety, and protocol adherence.

Responsibilities

• Serve as a clinical team member assigned to data review for clinicians, including verification of subject eligibility based on medical history
• Critically apply protocol-defined study requirements to assess data relevant to study endpoints (e.g., safety, tolerability, immunogenicity, efficacy)
• Review serious and non-serious adverse events (AEs), including drafting and responding to site queries and ensuring accurate and timely reconciliation of safety data
• Review reactogenicity data in eDiaries or EDC systems to ensure compliance with protocol-specified safety surveillance and monitoring
• Assist the lead clinician with aggregate data review and interpretation, preparation and management of safety narratives, and slide development for internal and external presentations
• Support additional study-related tasks such as literature reviews, data cleaning, and review of training materials
• Participate in safety surveillance meetings and contribute to PowerPoint creation as needed
• Be available during normal business hours for the assigned region and work the specified number of hours per week

Requirements

• Medical degree (MD, DO, MBBS, or equivalent)
• 2+ years of direct patient care experience post-residency
• Prior experience as a medical monitor
• Experience with safety data review (non-serious and serious AEs)
• Experience on an interventional clinical trial within the past 3 years
• Comfortable with complex medical reviews involving pediatric, adult, and obstetrical populations

Qualifications

• MD, DO, MBBS, or equivalent
• 2+ years of experience seeing patients post-residency

Nice to Have

• Experience with Family Medicine, Internal Medicine, Obstetrics and Gynecology, or Pediatrics
• Vaccine trials experience
• Familiarity with EDC platforms (InForm or RedCap)
• Experience with J Review or a similar data review system
• Training and experience in infectious diseases and/or infection control in a hospital setting

Skills

* Required skills

Benefits