Collabera

Title: Medical Monitor/Medical Director - Remote

Location: North Chicago, IL (Remote)

Specialties: Neurology, Psychiatry

Base: $80-$110/hr

Summary

Supports the clinical development Neuroscience team by providing medical and safety monitoring for clinical trials focused on neurodegenerative diseases such as Parkinson's, Alzheimer's, and Dementia. Responsibilities include medical monitoring of studies, reviewing safety data and serious adverse events, participating in safety meetings, reviewing clinical study reports and other documentation, and conducting literature reviews as requested.

Added on: 06/12/2025

Full Job Description

Position Details:
Industry: Pharmaceutical
Job Title: Medical Monitor/Medical Director - Remote Role
Duration: 12+ Months Contract (+ Potential Extension)
 
 
Pay Range: $80-$110/hr
 
Overview:
 


Responsible for supporting the clinical development Neuroscience team with medical and safety monitoring.


Neuroscience Group - 3 subgroups - Psychiatry, neurodegeneration and toxins. This role is with Neurodegeneration subgroup including diseases like Parkinsons, Alzheimer's, Dementia etc.


 
Responsibilities:


Provides medical monitoring and observation of clinical trials to ensure safety and adherence to protocol.


Coordinates, conducts, and communicates overview of safety data and significant changes to the study team.


Provide medical review, comment and assessment of causality for Serious Adverse Events (SAEs)


Responsible for medical monitoring of assigned studies including data reviews, queries assigned 


Participates in Product Safety Team meetings


Reviews CSRs/IBs/submissions, etc.


Peer review draft DRC materials


Monitor and compile competitive intelligence (landscape) assessments/white papers and provide medical perspective/implications


Assesses start-up requirements for EDC to ensure studies are set up properly for medical monitoring in collaboration with study team.


Conducts literature reviews at the request of study teams


 
Qualifications:


MD/DO with 2+ years clinical development experience conducting medical monitoring for clinical trials.


Excellent communication and interpersonal skills


Ability to work independently


Experience with Patient Reported Outcomes is preferred.