Associate Medical Director, Medical Safety Review (Remote)
Posted on Sep 26, 2024 by AbbVie
Mettawa, IL
Admin & Secretarial
Immediate Start
Annual Salary
Full-Time
- Remote
Job Description
Purpose:
The primary focus of this position is the medical review of clinical trial serious adverse events (SAEs) including causality assessment and company analysis development.
Main Responsibilities:
Performs causality assessment of adverse events in post-marketing individual case safety reports.
Performs medical review of clinical serious adverse events (SAEs).
Develops company analysis for suspected unexpected serious adverse reactions (SUSARs).
Responsible for accurate and timely communication with all clinical trial stakeholders.
May serve as secondary lead for therapeutic area.
Understands safety profile of assigned AbbVie products and development compounds as well as safety aspects of relevant therapeutic area drugs and patient populations.
Understands disease state for each indication within assigned AbbVie products and development compounds.
Understands global regulations, processes and practices.
Contributes as requested to PSEQ initiatives and deliverables.
This role can be remote in the United States.
Purpose:
The primary focus of this position is the medical review of clinical trial serious adverse events (SAEs) including causality assessment and company analysis development.
Main Responsibilities:
Performs causality assessment of adverse events in post-marketing individual case safety reports.
Performs medical review of clinical serious adverse events (SAEs).
Develops company analysis for suspected unexpected serious adverse reactions (SUSARs).
Responsible for accurate and timely communication with all clinical trial stakeholders.
May serve as secondary lead for therapeutic area.
Understands safety profile of assigned AbbVie products and development compounds as well as safety aspects of relevant therapeutic area drugs and patient populations.
Understands disease state for each indication within assigned AbbVie products and development compounds.
Understands global regulations, processes and practices.
Contributes as requested to PSEQ initiatives and deliverables.
This role can be remote in the United States.
Reference: 202502456
https://jobs.careeraddict.com/post/95584835
Associate Medical Director, Medical Safety Review (Remote)
Posted on Sep 26, 2024 by AbbVie
Mettawa, IL
Admin & Secretarial
Immediate Start
Annual Salary
Full-Time
- Remote
Job Description
Purpose:
The primary focus of this position is the medical review of clinical trial serious adverse events (SAEs) including causality assessment and company analysis development.
Main Responsibilities:
Performs causality assessment of adverse events in post-marketing individual case safety reports.
Performs medical review of clinical serious adverse events (SAEs).
Develops company analysis for suspected unexpected serious adverse reactions (SUSARs).
Responsible for accurate and timely communication with all clinical trial stakeholders.
May serve as secondary lead for therapeutic area.
Understands safety profile of assigned AbbVie products and development compounds as well as safety aspects of relevant therapeutic area drugs and patient populations.
Understands disease state for each indication within assigned AbbVie products and development compounds.
Understands global regulations, processes and practices.
Contributes as requested to PSEQ initiatives and deliverables.
This role can be remote in the United States.
Purpose:
The primary focus of this position is the medical review of clinical trial serious adverse events (SAEs) including causality assessment and company analysis development.
Main Responsibilities:
Performs causality assessment of adverse events in post-marketing individual case safety reports.
Performs medical review of clinical serious adverse events (SAEs).
Develops company analysis for suspected unexpected serious adverse reactions (SUSARs).
Responsible for accurate and timely communication with all clinical trial stakeholders.
May serve as secondary lead for therapeutic area.
Understands safety profile of assigned AbbVie products and development compounds as well as safety aspects of relevant therapeutic area drugs and patient populations.
Understands disease state for each indication within assigned AbbVie products and development compounds.
Understands global regulations, processes and practices.
Contributes as requested to PSEQ initiatives and deliverables.
This role can be remote in the United States.
Reference: 202502456
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