Medical Safety Physician
Lincolnton, NC ยท Remote
Medical Safety Physician 6-month assignment 100% Remote What are the three most important qualifications: Argus experience, self starter, experience in pharmacovigilance and infection disease ...
Lincolnton, NC ยท Remote
Medical Safety Physician 6-month assignment 100% Remote What are the three most important qualifications: Argus experience, self starter, experience in pharmacovigilance and infection disease ...
Lincolnton, NC ยท Remote
Medical Safety Physician 6-month assignment 100% Remote What are the three most important qualifications: Argus experience, self starter, experience in pharmacovigilance and infection disease ...
The Director, Medical Safety (Scientist) is a key member of the Medical Safety team, and provides leadership, line management, and/or mentorship for the junior safety scientists within Medical Safety ...
The Director, Medical Safety (Scientist) is a key member of the Medical Safety team, and provides leadership, line management, and/or mentorship for the junior safety scientists within Medical Safety ...
Redwood City, CA ยท On-site
$298K - $350K/yr
Medical Safety Leadership * Define and drive the medical safety strategy across the portfolio * Provide senior medical safety leadership for safety interpretation and benefit-risk assessment * Ensure ...
Redwood City, CA ยท On-site
$298K - $350K/yr
Medical Safety Leadership * Define and drive the medical safety strategy across the portfolio * Provide senior medical safety leadership for safety interpretation and benefit-risk assessment * Ensure ...
The Director, Medical Safety (Scientist) is a key member of the Medical Safety team, and provides leadership, line management, and/or mentorship for the junior safety scientists within Medical Safety ...
The Director, Medical Safety (Scientist) is a key member of the Medical Safety team, and provides leadership, line management, and/or mentorship for the junior safety scientists within Medical Safety ...
As a Principal Medical Safety Specialist (Pr. MSS) you will have an integral role in the day-to-day functioning of the global medical safety organization. In this vital role you will execute upon ...
As a Principal Medical Safety Specialist (Pr. MSS) you will have an integral role in the day-to-day functioning of the global medical safety organization. In this vital role you will execute upon ...
Learn more at The Pharmaceuticals Medical Safety Officer (MSO) has accountability for assessing the medical safety of assigned products and will strategically lead cross-functional matrix teams ...
Learn more at The Pharmaceuticals Medical Safety Officer (MSO) has accountability for assessing the medical safety of assigned products and will strategically lead cross-functional matrix teams ...
Foster City, CA ยท On-site
$215 - $230/hr
Represent Medical Safety Science in assigned clinical study team meetings for Mirum products * Support the Sr. Director of Medical Safety in Safety Adjudication Meetings, as necessary * Review and ...
New
Foster City, CA ยท On-site
$215 - $230/hr
Represent Medical Safety Science in assigned clinical study team meetings for Mirum products * Support the Sr. Director of Medical Safety in Safety Adjudication Meetings, as necessary * Review and ...
New
Learn more at The Pharmaceuticals Medical Safety Officer (MSO) has accountability for assessing the medical safety of assigned products and will strategically lead cross-functional matrix teams ...
Learn more at The Pharmaceuticals Medical Safety Officer (MSO) has accountability for assessing the medical safety of assigned products and will strategically lead cross-functional matrix teams ...
Provide Medical Safety/PV inputs to the assigned products at Jazz Pharmaceuticals, which may include Clinical Development program of all phases, Investigator Sponsored, Compassionate Use, and Disease ...
Provide Medical Safety/PV inputs to the assigned products at Jazz Pharmaceuticals, which may include Clinical Development program of all phases, Investigator Sponsored, Compassionate Use, and Disease ...
Foster City, CA ยท Hybrid
$215K - $230K/yr
POSITION SUMMARY Mirum Pharmaceutical is seeking an Associate Director of Medical Safety Science (Safety Scientist). The ideal candidate will have experience in and perform multiple activities ...
Foster City, CA ยท Hybrid
$215K - $230K/yr
POSITION SUMMARY Mirum Pharmaceutical is seeking an Associate Director of Medical Safety Science (Safety Scientist). The ideal candidate will have experience in and perform multiple activities ...
... Medical Director / Global Safety Physician is responsible for implementing the global safety ... This includes generating all major pre- and post-marketing safety deliverables including signal ...
... Medical Director / Global Safety Physician is responsible for implementing the global safety ... This includes generating all major pre- and post-marketing safety deliverables including signal ...
... Medical Director / Global Safety Physician is responsible for implementing the global safety ... This includes generating all major pre- and post-marketing safety deliverables including signal ...
... Medical Director / Global Safety Physician is responsible for implementing the global safety ... This includes generating all major pre- and post-marketing safety deliverables including signal ...
Provide Medical Safety/PV inputs to the assigned products at Jazz Pharmaceuticals, which may include Clinical Development program of all phases, Investigator Sponsored, Compassionate Use, and Disease ...
Provide Medical Safety/PV inputs to the assigned products at Jazz Pharmaceuticals, which may include Clinical Development program of all phases, Investigator Sponsored, Compassionate Use, and Disease ...
... Medical Director / Global Safety Physician is responsible for implementing the global safety ... This includes generating all major pre- and post-marketing safety deliverables including signal ...
... Medical Director / Global Safety Physician is responsible for implementing the global safety ... This includes generating all major pre- and post-marketing safety deliverables including signal ...
$149K - $237K/yr
The Medical Safety Manager, Enterprise Informatics (EI) responsible for conducting comprehensive evaluations of safety information sourced form a variety of channels such as Post-Marketing ...
$149K - $237K/yr
The Medical Safety Manager, Enterprise Informatics (EI) responsible for conducting comprehensive evaluations of safety information sourced form a variety of channels such as Post-Marketing ...
Bismarck, ND ยท On-site
Senior Director, Global Medical Safety physician (psychedelics), leads and supports safety team(s) in all aspects of pharmacovigilance and risk management activities for assigned products, both ...
New
Bismarck, ND ยท On-site
Senior Director, Global Medical Safety physician (psychedelics), leads and supports safety team(s) in all aspects of pharmacovigilance and risk management activities for assigned products, both ...
New
Sacramento, CA ยท On-site
Senior Director, Global Medical Safety physician (psychedelics), leads and supports safety team(s) in all aspects of pharmacovigilance and risk management activities for assigned products, both ...
New
Sacramento, CA ยท On-site
Senior Director, Global Medical Safety physician (psychedelics), leads and supports safety team(s) in all aspects of pharmacovigilance and risk management activities for assigned products, both ...
New
Carson City, NV ยท On-site
Senior Director, Global Medical Safety physician (psychedelics), leads and supports safety team(s) in all aspects of pharmacovigilance and risk management activities for assigned products, both ...
New
Carson City, NV ยท On-site
Senior Director, Global Medical Safety physician (psychedelics), leads and supports safety team(s) in all aspects of pharmacovigilance and risk management activities for assigned products, both ...
New
The MSO will communicate potential and known risks, when appropriate, to TA Safety Head, Chief Safety Officer (CSO), Chief Medical Officer (CMO), Qualified Person for Pharmacovigilance (QPPV), Senior ...
The MSO will communicate potential and known risks, when appropriate, to TA Safety Head, Chief Safety Officer (CSO), Chief Medical Officer (CMO), Qualified Person for Pharmacovigilance (QPPV), Senior ...
Senior Director, Global Medical Safety physician (psychedelics), leads and supports safety team(s) in all aspects of pharmacovigilance and risk management activities for assigned products, both ...
Senior Director, Global Medical Safety physician (psychedelics), leads and supports safety team(s) in all aspects of pharmacovigilance and risk management activities for assigned products, both ...
$73K - $88.7K
22% of jobs
$91.3K is the 25th percentile. Wages below this are outliers.
$88.7K - $104.5K
19% of jobs
$104.5K - $120.2K
0% of jobs
$120.2K - $135.9K
0% of jobs
$135.9K - $151.6K
0% of jobs
$151.6K - $167.4K
0% of jobs
$167.4K - $183.1K
6% of jobs
The median wage is $186.7K / yr.
$183.1K - $198.8K
14% of jobs
$206.7K is the 75th percentile. Wages above this are outliers.
$198.8K - $214.5K
29% of jobs
$214.5K - $230.3K
5% of jobs
$230.3K - $246K
5% of jobs
$73K
$162.4K
$246K
| Aspect | Medical Safety | Medical Compliance |
|---|---|---|
| Required Credentials | Certifications in safety management, healthcare regulations | Certifications in healthcare laws, regulatory standards |
| Work Environment | Hospitals, pharmaceutical companies, clinical settings | Healthcare facilities, regulatory agencies, pharmaceutical firms |
| Employer & Industry Usage | Focuses on patient and staff safety protocols | Ensures adherence to legal and regulatory standards |
Medical Safety and Medical Compliance roles often overlap but serve different focuses. Medical Safety emphasizes preventing hazards and ensuring safety protocols, while Medical Compliance centers on adhering to laws and regulations. Both are vital in healthcare settings, but their primary goals and certifications differ slightly.

Medical Safety Physician
6-month assignment
100% Remote
What are the three most important qualifications: Argus experience, self starter, experience in pharmacovigilance and infection disease vaccines
Licenses/Certifications: A Valid medical license (active or inactive), or equivalent, from the country or region in which he/she resides and works
Description
Delivers medical, clinical and scientific advisory expertise in clinical research studies and post marketing programs (RWI). Signal detection and aggregated reporting.
Provides medical, scientific and therapeutic expertise on pharmacovigilance services.
Participates in all aspects of the Medical Safety activities as per scope of work, such as performing medical review and clarification of trial-related Adverse Events including review of analysis of similar events, medical evaluation of post-marketing adverse drug reactions, review medical inputs for into signal management and benefit-risk evaluation of drugs in clinical trial and post marketing set up, safety aggregate report review, safety review of study protocol, investigators brochure and other reference safety information, clinical study report narrative review, providing medical assessment comments etc. and serving as an internal consultant for any medical support for pharmacovigilance operations.
Responsibilities
Essential Functions
Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary
Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements
Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported
Provide aggregate reviews of safety information, including clinical data, to maintain oversight of a product's safety profile
Provide coding review of AEs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data
Represent safety and clinical data review findings during client meetings
Provide medical review and edits to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports
Provide medical review and edits of Development Risk Management Plans, EU Risk Management Plans or US Risk
Evaluation and Mitigation Strategies
Provide medical oversight for label development, review and change
Provide medical support and attendance at Data Safety Monitoring Board Meetings
Attends and contributes medical safety evaluation on Safety Monitoring Committees
Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document
Provide medical review and edits to Drug Safety Reports or other benefit-risk assessments
Review and sign off on both the Project Safety Plan and the Medical Monitoring Plan per medical safety scope agreed in contract
Perform Medical Safety review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs) for appropriate safety content and data capture.
Act as Global Safety Physician or Assistant or Back-up on projects as assigned
Attend project meetings, medical safety team meetings, and client meetings as requested
Ensure coverage for all medical safety deliverables within regulatory or contracted timelines
Provide medical escalation support for medical information projects
Provide medical escalation support for EU Qualified Persons for Pharmacovigilance projects
24 hour medical support as required on assigned projects
Maintain awareness of medical-safety-regulatory industry developments
Experience
Typically requires 5 - 7 years of prior relevant experience.
Knowledge
Requires deep knowledge of one or more related job areas typically obtained through advanced education combined with experience.
Typically viewed as having a specialty within discipline.
Education: A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
Skills & Abilities:
Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including
knowledge of regulations and guidelines pertaining to safety and good clinical practice
Knowledge of clinical trials and pharmaceutical research process
Ability to establish and meet priorities, deadlines, and objectives.
Skills in providing consultation and advice on multiple assignments required, as well as initiative and flexibility
Ability to establish and maintain effective working relationships with coworkers, managers and clients
Physical Demands:
Sit at a desk or table with some walking, standing, bending, stooping, or carrying of light objects.
Perform continuous operation of a personal computer for four hours or more.
Use hands and fingers to handle and manipulate objects and/or operate equipment.
All your information will be kept confidential according to EEO guidelines.
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1,001 - 5,000 Employees
Raleigh, NC, US
2004