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Icsr Jobs (NOW HIRING)

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 ...

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

$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 ...

Section Details / Example Content Domain Healthcare/Pharma Case processing (ICSR) Soft Skills - Excellent communication - Team collaboration - Documentation and knowledge sharing Education ...

Showing results 41-60

Icsr information

See salary details

$12

$49

$85

How much do icsr jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for icsr in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

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:

Infographic showing various Icsr job openings in the United States as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 77% Physical, 6% Hybrid, and 17% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

GPV Functional QA Sr. Consultant

Deloitte

Princeton, NJ • On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.


Deloitte rating

8.2

Company rating: 8.2 out of 10

Based on 93 frontline employees who took The Breakroom Quiz

46th of 152 rated financial services


Job description

Are you an experienced, passionate pioneer in technology who wants to work in a collaborative environment? As an experienced Global Pharmacovigilance Functional QA Senior Consultant you will have the ability to share new ideas and collaborate on projects as a consultant without the extensive demands of travel. If so, consider an opportunity with Deloitte under our Project Talent Model. Project Talent Model (PTM) is a talent model that is tailored specifically for long-term, onsite client service delivery.
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
The Team
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
The wage range for this role takes into account the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Deloitte, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current range is $120,200 - $145,000.
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.
Recruiting tips
From developing a stand out resume to putting your best foot forward in the interview, we want you to feel prepared and confident as you explore opportunities at Deloitte. Check out recruiting tips from Deloitte recruiters.
Benefits
At Deloitte, we know that great people make a great organization. We value our people and offer employees a broad range of benefits. Learn more about what working at Deloitte can mean for you.
Our people and culture
Our inclusive culture empowers our people to be who they are, contribute their unique perspectives, and make a difference individually and collectively. It enables us to leverage different ways of thinking, ideas, and perspectives, and bring more creativity and innovation to help solve our clients' most complex challenges. This makes Deloitte one of the most rewarding places to work.
Our purpose
Deloitte's purpose is to make an impact that matters for our people, clients, and communities. At Deloitte, purpose is synonymous with how we work every day. It defines who we are. Our purpose comes through in our work with clients that enables impact and value in their organizations, as well as through our own investments, commitments, and actions across areas that help drive positive outcomes for our communities. Learn more.
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

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