Core systems include AVISSO (Argus), Empirica Signals and Topics, Global Intake Tool, MedDRA Coding Tool, ICSR Reporting Rule Survey, RMS-RSI, SLARDS, and TransformPV. The candidate must understand ...
Core systems include AVISSO (Argus), Empirica Signals and Topics, Global Intake Tool, MedDRA Coding Tool, ICSR Reporting Rule Survey, RMS-RSI, SLARDS, and TransformPV. The candidate must understand ...
Senior Specialist, Drug Safety
South Boston, MA · On-site
$105K - $115K/yr
Position Summary Reporting to the Head of PV Ops, the Senior Specialist, Drug Safety will support individual case safety report (ICSR) processing and ensure a high level of quality of safety cases.
Senior Specialist, Drug Safety
South Boston, MA · On-site
$105K - $115K/yr
Position Summary Reporting to the Head of PV Ops, the Senior Specialist, Drug Safety will support individual case safety report (ICSR) processing and ensure a high level of quality of safety cases.
Oversee daytoday ICSR case management operations, including maintaining oversight reports to monitor quality, performance, and compliance. * Ensure compliance with internal procedures and global ...
Oversee daytoday ICSR case management operations, including maintaining oversight reports to monitor quality, performance, and compliance. * Ensure compliance with internal procedures and global ...
May perform initial data entry of ICSRs (review, extract, accurately enter AE data from ICSR reports). May interpret case-related information including medical conditions, lab results and procedures ...
May perform initial data entry of ICSRs (review, extract, accurately enter AE data from ICSR reports). May interpret case-related information including medical conditions, lab results and procedures ...
Support ICSR submissions and transmissions as needed. * Perform CRO case QC activities, reconciliation etc as required. * Work on highest priority or assigned cases using Workflow Management System ...
Quick apply
Support ICSR submissions and transmissions as needed. * Perform CRO case QC activities, reconciliation etc as required. * Work on highest priority or assigned cases using Workflow Management System ...
Review, extract and accurately enter AE data from ICSR reports from both investigational and post marketing products. Interpret case-related information including medical conditions, lab results and ...
Review, extract and accurately enter AE data from ICSR reports from both investigational and post marketing products. Interpret case-related information including medical conditions, lab results and ...
Drug Safety Scientist
Clayton, NC · On-site
$90 - $130/hr
Individual Case Safety Report (ICSR) submission manager assigning submissions and providing supervision and oversight of expedited submissions ensuring that all ICDRs are identified and submissions ...
New
Drug Safety Scientist
Clayton, NC · On-site
$90 - $130/hr
Individual Case Safety Report (ICSR) submission manager assigning submissions and providing supervision and oversight of expedited submissions ensuring that all ICDRs are identified and submissions ...
New
Senior Specialist, Drug Safety
$105K - $115K/yr
Position Summary Reporting to the Head of PV Ops, the Senior Specialist, Drug Safety will support individual case safety report (ICSR) processing and ensure a high level of quality of safety cases.
Senior Specialist, Drug Safety
$105K - $115K/yr
Position Summary Reporting to the Head of PV Ops, the Senior Specialist, Drug Safety will support individual case safety report (ICSR) processing and ensure a high level of quality of safety cases.
$105 - $115/hr
Reporting to the Head of PV Ops, the Senior Specialist, Drug Safety will support individual case safety report (ICSR) processing and ensure a high level of quality of safety cases. The successful ...
$105 - $115/hr
Reporting to the Head of PV Ops, the Senior Specialist, Drug Safety will support individual case safety report (ICSR) processing and ensure a high level of quality of safety cases. The successful ...
Senior Specialist, Drug Safety
Boston, MA · On-site
$105 - $115/hr
Position SummaryReporting to the Head of PV Ops, the Senior Specialist, Drug Safety will support individual case safety report (ICSR) processing and ensure a high level of quality of safety cases.
Senior Specialist, Drug Safety
Boston, MA · On-site
$105 - $115/hr
Position SummaryReporting to the Head of PV Ops, the Senior Specialist, Drug Safety will support individual case safety report (ICSR) processing and ensure a high level of quality of safety cases.
... ICSR, DoDAF, and JITC conformance and governance processes. • Familiarity with Joint Requirements Oversight Council (JROC) and/or the Joint Capabilities Integration and Development System (JCIDS ...
... ICSR, DoDAF, and JITC conformance and governance processes. • Familiarity with Joint Requirements Oversight Council (JROC) and/or the Joint Capabilities Integration and Development System (JCIDS ...
Senior Clinical Trial Case Manager
King Of Prussia, PA · On-site
$120 - $180/hr
Leads or oversees ICSR reporting compliance analyses, liaises internally and externally to meet regulatory reporting requirements, and prepares Suspected Unexpected Serious Adverse Reactions for ...
New
Senior Clinical Trial Case Manager
King Of Prussia, PA · On-site
$120 - $180/hr
Leads or oversees ICSR reporting compliance analyses, liaises internally and externally to meet regulatory reporting requirements, and prepares Suspected Unexpected Serious Adverse Reactions for ...
New
Executive Director, Global Patient Safety Sciences - Rare Disease
Tarrytown, NY · On-site
$286 - $476/hr
Act as a resource for medical review for complex ICSR data sources of assigned compounds and serve as point of escalation for ICSR causality assessments. * Provide oversight for safety signal ...
New
Executive Director, Global Patient Safety Sciences - Rare Disease
Tarrytown, NY · On-site
$286 - $476/hr
Act as a resource for medical review for complex ICSR data sources of assigned compounds and serve as point of escalation for ICSR causality assessments. * Provide oversight for safety signal ...
New
(Senior-) Director Head of Medical Review (Pharmacovigilance)
Cambridge, MA · On-site
$168 - $318/hr
Comprehensive knowledge of global pharmacovigilance regulations (ICH, GVP) and hands‑on ICSR processing experience. * Proficiency with safety databases (e.g., Veeva Vault Safety). * Strong ...
(Senior-) Director Head of Medical Review (Pharmacovigilance)
Cambridge, MA · On-site
$168 - $318/hr
Comprehensive knowledge of global pharmacovigilance regulations (ICH, GVP) and hands‑on ICSR processing experience. * Proficiency with safety databases (e.g., Veeva Vault Safety). * Strong ...
Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports ( e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g ...
Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports ( e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g ...
Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports ( e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g ...
Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports ( e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g ...
Veeva Safety Specialist
OR · Remote
Section Details / Example Content Domain Healthcare/Pharma Case processing (ICSR) Soft Skills - Excellent communication - Team collaboration - Documentation and knowledge sharing Education ...
Quick apply
Veeva Safety Specialist
OR · Remote
Section Details / Example Content Domain Healthcare/Pharma Case processing (ICSR) Soft Skills - Excellent communication - Team collaboration - Documentation and knowledge sharing Education ...
Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports ( e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g ...
Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports ( e.g. PBRER, PSUR, DSUR) as well as other client deliverables (e.g ...
Pharmacovigilance Scientist
Horsham, PA · On-site
May Triage and classify ICSRs for report type, seriousness, causality, expectedness/labeling and reporting; prioritize ICSR according to regulatory requirements *Confirmation of Safety Coordinator ...
Pharmacovigilance Scientist
Horsham, PA · On-site
May Triage and classify ICSRs for report type, seriousness, causality, expectedness/labeling and reporting; prioritize ICSR according to regulatory requirements *Confirmation of Safety Coordinator ...
Support and oversee all vendor activity related to individual case safety reports (ICSR) and case processing, aggregate reports (DSUR, PSUR, and PADERs), expedited reporting, safety database ...
Support and oversee all vendor activity related to individual case safety reports (ICSR) and case processing, aggregate reports (DSUR, PSUR, and PADERs), expedited reporting, safety database ...
Icsr information
See salary details
$12.26 - $18.95
7% of jobs
$18.95 - $25.63
4% of jobs
$25.63 - $32.32
3% of jobs
$38.25 is the 25th percentile. Wages below this are outliers.
$32.32 - $39.01
12% of jobs
The median wage is $44.20 / hr.
$39.01 - $45.69
31% of jobs
$45.69 - $52.38
15% of jobs
$54.36 is the 75th percentile. Wages above this are outliers.
$52.38 - $59.07
12% of jobs
$59.07 - $65.76
0% of jobs
$65.76 - $72.44
9% of jobs
$72.44 - $79.13
5% of jobs
$79.13 - $85.82
2% of jobs
$12
$49
$85
How much do icsr jobs pay per hour?
What is an ICSR?
An ICSR (Individual Case Safety Report) job involves the processing and reviewing of adverse event reports related to pharmaceutical products or medical devices. Professionals in this role ensure that safety data is accurately documented and reported to regulatory authorities in compliance with guidelines such as those from the FDA, EMA, or ICH. They analyze case information, categorize adverse events, and contribute to pharmacovigilance efforts to enhance patient safety.
What does an ICSR do?
ICSR professionals are responsible for collecting, evaluating, and processing adverse event reports from various sources such as healthcare professionals, patients, and clinical trials. Their daily tasks often include data entry into specialized safety databases, coding of medical terms (using MedDRA), preparing case narratives, and ensuring timely submission of safety reports to regulatory authorities. Collaboration with safety physicians, regulatory teams, and quality assurance colleagues is common, as accuracy and compliance are essential. This role requires managing multiple cases simultaneously while maintaining high standards for data integrity and regulatory timelines.
What are the key skills and qualifications needed to thrive as an ICSR?
To thrive as an ICSR (Individual Case Safety Report) professional, you need strong attention to detail, a background in life sciences or pharmacy, and familiarity with pharmacovigilance practices. Proficiency in safety databases (such as ArisG or Oracle Argus), MedDRA coding, and regulatory reporting requirements is highly valuable, and some roles may prefer certification in pharmacovigilance. Excellent organizational skills, critical thinking, and clear written communication help ensure thorough and accurate case processing. These abilities are crucial to maintaining regulatory compliance, ensuring patient safety, and supporting effective drug safety monitoring.
What are the most commonly searched types of Icsr jobs?
The most popular types of Icsr jobs are:
What states have the most Icsr jobs?
States with the most job openings for Icsr jobs include:
What job categories do people searching Icsr jobs look for?
The top searched job categories for Icsr jobs are:

Full-time
This job post has expired 1 day ago. Applications are no longer accepted.
Deloitte rating
8.2
Based on 93 frontline employees who took The Breakroom Quiz
46th of 152 rated financial services
Job description
Recruiting for this role ends on 9/11/2026
Work you'll do/Responsibilities
The Global Pharmacovigilance Functional QA Senior Consultant will Lead the onsite testing lead for Global Pharmacovigilance (GPV) tower - a 16-application portfolio covering the full PV case lifecycle from adverse event intake through signal detection and aggregate reporting. Core systems include AVISSO (Argus), Empirica Signals and Topics, Global Intake Tool, MedDRA Coding Tool, ICSR Reporting Rule Survey, RMS-RSI, SLARDS, and TransformPV. The candidate must understand the pharmacovigilance data flow and be comfortable leading client-facing interactions, driving UAT coordination, and ensuring release readiness in a GxP-regulated environment with zero-defect tolerance. Serve as the onsite testing lead for the GPV tower, acting as the primary interface between the testing team and GPV business stakeholders, project managers, and release governance forums. Develop and execute test strategy and plans for GxP-regulated PV applications in alignment with CSA/CSV methodology and Functional Risk Assessment (FRA) outcomes. Design and execute test scenarios across SIT, UAT, OQ, and PQ phases for safety database (AVISSO), signal detection (Empirica), intake (Global Intake Tool), coding (MedDRA), and reporting systems (ICSR Rules, SLARDS). Lead UAT coordination - scheduling, entry/exit criteria, business SME participation, and timely sign-off. Own defect lifecycle management including triage, root cause discussion, stakeholder communication, and closure. Prepare and present testing status reports, defect dashboards, and release readiness assessments to client stakeholders. Proactively escalate testing risks and issues with clear ownership and resolution timelines. Operate within ALM/ALVIS for test planning, execution tracking, and evidence capture. The successful candidate would possess these skills:
- Ability to work independently and collaborate as part of a team
- Effective written and verbal communication skills
- Meticulous attention to detail and quality of work product
- Ability to build and sustain professional relationships
- Ability to lead projects or workstreams
- Ability to manage and prioritize multiple tasks in a fast-paced and dynamic environment
- Strong interpersonal skills and professional demeanor
- Ability to meet deadlines
- Ability to provide clear guidance to others
AI & Engineering leverages cutting-edge engineering capabilities to build, deploy, and operate integrated/verticalized sector solutions in software, data, AI, network, and hybrid cloud infrastructure. These solutions are powered by engineering for business advantage, transforming mission-critical operations. We enable clients to stay ahead with the latest advancements by transforming engineering teams and modernizing technology & data platforms. Our delivery models are tailored to meet each client's unique requirements
Our Industry Solutions offering provides verticalized solutions that transform how clients sell products, deliver services, generate growth, and execute mission-critical operations. We deliver integrated business expertise with scalable, repeatable technology solutions specifically engineered for each sector.
Qualifications Required
- 5+ years of onsite testing for the GPV tower, acting as the primary interface between the testing team and GPV business stakeholders, project managers, and release governance forums.
- Develop and execute test strategy and plans for GxP-regulated PV applications in alignment with CSA/CSV methodology and Functional Risk Assessment (FRA) outcomes.
- Design and execute test scenarios across SIT, UAT, OQ, and PQ phases for safety database (AVISSO), signal detection (Empirica), intake (Global Intake Tool), coding (MedDRA), and reporting systems (ICSR Rules, SLARDS).
- Lead UAT coordination - scheduling, entry/exit criteria, business SME participation, and timely sign-off.
- Operate within ALM/ALVIS for test planning, execution tracking, and evidence capture.
- Bachelor's degree, preferably in information technology, business, or healthcare related field; or equivalent experience
- Limited immigration sponsorship may be available
- Ability to travel 10%, on average, based on the work you do and the clients and industries/sectors you serve
You may also be eligible to participate in a discretionary annual incentive program, subject to the rules governing the program, whereby an award, if any, depends on various factors, including, without limitation, individual and organizational performance.
Deloitte is committed to providing reasonable accommodations for people with disabilities. If you require a reasonable accommodation to participate in the recruiting process, please direct your inquiries to the Global Call Center (GCC) at USTalentCICInbox@deloitte.com.
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Professional development
From entry-level employees to senior leaders, we believe there's always room to learn. We offer opportunities to build new skills, take on leadership opportunities and connect and grow through mentorship. From on-the-job learning experiences to formal development programs, our professionals have a variety of opportunities to continue to grow throughout their career.
As used in this posting, "Deloitte" means Deloitte Consulting LLP, a subsidiary of Deloitte LLP. Please see https://www.deloitte.com/us/about for a detailed description of the legal structure of Deloitte LLP and its subsidiaries.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or protected veteran status, or any other legally protected basis, in accordance with applicable law.
Requisition code: 358936
Job ID 358936
About Deloitte
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Industry
Finance and insurance and business management consulting
Company size
10,000+ Employees
Headquarters location
Orlando, FL, US