Medical Monitor

Davita Inc.; Avon (IL); Remote; USD 100,000 - 150,000; Full time

Job summary

A leading company is seeking a Medical Monitor to support their Neuroscience clinical development team. This remote position involves overseeing clinical trials to ensure safety and adherence to protocols, along with data review and assessment of Serious Adverse Events. Candidates must possess an MD/DO and relevant clinical monitoring experience, making this an exceptional opportunity for professionals looking to impact clinical research significantly.

Qualifications

• MD/DO with clinical development experience in medical monitoring for clinical trials.
• Experience with late-stage trials preferred.

Responsibilities

• Provides medical monitoring and observation of clinical trials.
• Coordinates and communicates overview of safety data.
• Reviews case safety reports, assessments for Serious Adverse Events (SAEs).
• Assesses start-up requirements for electronic data capture systems.

Skills

Medical Monitoring experience

Excellent communication skills

Interpersonal skills

Ability to work independently

Education

MD/DO

2+ years clinical development experience

Job description

Job title: Medical Monitor

Location: Remote

Duration: 12 Months



Purpose:

Describe the primary goals, objectives or functions or outputs of this position.

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



Responsibilities:

List up to 10 main responsibilities for the job. Include information about the accountability and scope.

* 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 in TESLA

* 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:

List required and preferred qualifications (up to 10). Include education, skills and experience.

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



What are the top 3-5 skills, experience or education required for this position:

1. Medical Monitoring experience (later stage trials preferred)

2. Excellent communication and interpersonal skills

3. Ability to work independently