Medical Monitor

I am currently working with a long standing client of mine that is looking to bring on a contract Medical Monitor for an ongoing clinical study of an investigational monoclonal antibody in sepsis. This is a high-impact opportunity for a clinician with deep ICU and sepsis expertise, strong clinical-research experience, and the ability to provide responsive, proactive medical oversight throughout an active study.
Responsibilities
Provide ongoing medical monitoring and oversight of participant progress, safety data, and emerging clinical issues.
Review adverse events, safety signals, laboratory data, and other clinically relevant participant information.
Respond promptly to protocol, eligibility, dosing, and participant-management questions from investigators and the study team.
Prepare clear, clinically rigorous participant case narratives and medical assessments for safety and dose-escalation reviews.
Present participant-level clinical information, safety findings, and medical assessments at Safety Review Committee and Data Safety Monitoring Board (DSMB) meetings.
Maintain close, effective communication with the investigator, sponsor, and cross-functional study team.
Rapidly become familiar with the study protocol and assume ownership of the medical-monitoring function for an already-enrolling clinical trial.
Remote
12 month Contract
Required Experience
MD with experience in Sepsis
Significant clinical expertise in intensive care medicine, critical care, emergency medicine, infectious diseases, or a closely related specialty.
Strong experience managing patients with sepsis, septic shock, and complex critical illness.
Prior experience in clinical development, clinical research, medical monitoring, or investigator-led/sponsor-led clinical trials.
Direct experience with sepsis clinical trials is strongly preferred.
Experience reviewing participant safety data, evaluating eligibility questions, and contributing to medical or safety governance discussions.
Comfortable presenting clinical and safety information to senior stakeholders, including Safety Review Committees and DSMBs.
Excellent clinical judgment, written communication, and ability to synthesize complex participant information into clear medical assessments.
Able to work independently, respond decisively to urgent issues, and collaborate effectively across investigator, sponsor, and study-team stakeholders.
Availability to support urgent matters outside routine business hours, including 24/7 telephone accessibility for participant-safety issues.

Work arrangement
Yes