Vertex Pharmaceuticals Inc (US) Posted August 28, 2026

Patient Safety ICSR Manager

Boston, United States Full time
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Vertex Pharmaceuticals Inc (US) is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Description

General Summary:

The Global Patient Safety Individual Case Safety Report (ICSR) Manager is responsible for performing Individual Case Safety Report (ICSR) processing activities, including case book-in, triage, case entry (structured field data-entry, event coding, narrative writing, and pursuit of follow-up information), finalization and reporting. The Global Patient Safety ICSR Manager works with a high degree of independence and is proficient at troubleshooting problems to create and execute improved internal procedures, and to ensure compliance with applicable regulatory requirements. This individual ensures that all work performed is in accordance with relevant regulatory guidelines. By virtue of their experience, the Global Patient Safety ICSR Manager is expected to provide guidance and leadership for ICSR processing and complete work in a resourceful, self-sufficient manner.

Key Duties and Responsibilities:

Performs workflow management activities, in addition to contributing in individual workflows

Monitors GPS Inbox for receipt of safety information

Performs initial ICSR book-in activities, including determination of a valid case as well as initial, follow-up, and duplicate information

Archives ICSR documentation received through the GPS inbox per applicable procedures

Reviews and interprets all new and follow-up safety information to determine the appropriate information to enter into the Global Safety Database

Responsible for the management of all assigned ICSRs from receipt to ICSR closure, including follow-up requests

Supports and/or executes timely reporting of ICSRs to Health Authorities/Regulatory Agencies and distribution of ICSRs to Vendors/Business Partners and other stakeholders as required

Performs periodic Global Safety Database searches to support inquiries from stakeholders as required

Performs case nullifications/deletions of ICSRs

Provides feedback on quality and other periodic reviews

Performs Business Partners and/or Vendor reconciliations and acts as a liaison as applicable

Ensures that all international regulations are followed regarding PV procedures

Assists in the creation of ad hoc safety reports for submission to relevant stakeholders

May conduct presentations of safety issues, initiatives and projects

Provides input on effectiveness of the safety management system and when applicable, provide suggestions for improvement of ICSR processing efficiency

Reviews and may be responsible for authoring Standard Operating Procedures (SOPs) and Working Instructions, with minimal supervision

Helps to identify key departmental needs and provides constructive input on solutions

Participates as a cross functional team member of Study Execution Teams

Interfaces with study sites to ensure complete, accurate, and timely reporting of safety information

Participates in Serious Adverse Event (SAE) Reconciliation activities

Assists in developing and maintaining PV agreements and manages relationships with Vendors/Business Partners

Mentors other Specialists and GPS staff

Performs other duties as assigned

Knowledge and Skills:

Proficient in Argus Safety

Embrace the application of AI solutions to simplify and build process efficiency

Sound ability to communicate effectively in a matrix environment

Ability to multi-task

Solid written and oral communication skills

Sound attention to detail

Strong sense of responsibility and an ability to work autonomously, as well as act as a strong team player

Displays ability to understand established procedures and communicate those procedures to others

Education and Experience:

B.S. (or equivalent degree) and 4 – 5 years of relevant work experience, or

PharmD, M.S.N (or equivalent degree) and 3 – 5 years of relevant work experience

Pay Range:

$121,600 - $182,400

Disclosure Statement:

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.  From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

Flex Designation:

Remote-Eligible

Flex Eligibility Status:

In this Remote-Eligible role, you can choose to be designated as:

1.    Remote: work remotely five days per week and come into the office on occasion – you’re always welcome on-site; or select

2.    Hybrid: work remotely up to two days per week; or select

3.    On-Site: work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

#LI-Remote

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

Job details

Seniority
Manager
Function
Pharmacovigilance
Therapeutic area
Not listed
Location
Boston, United States
Employment type
Full time

How this role compares

Computed from every other active Pharmacovigilance role in our database, not just this employer's listings.

We currently track 38 comparable Manager Pharmacovigilance roles across 24 biopharma companies.

38Comparable roles tracked
37Currently active
24Companies hiring similar roles
18Countries represented

Salary context

4 of 38 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $121,600/yr – $182,400/yr
Lowest disclosed · Manager, Pharmacovigilance Case Processing (Boston, MA, US) · Servier $131,000/yr – $150,000/yr
Peer group range $140,500 – $199,500 (median $166,250)

Where these roles are based

Top locations among the 38 comparable roles

United States10
India4
Poland3
Japan3
France3
China2

+ 12 more countries

Seniority mix

38 of 38 peers have a known seniority level

Manager24
Associate Director9
Associate5

Therapeutic area mix

0 of 38 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Amgen Inc. Remote, United States Manager
Same function Same seniority Same country
60%similar
Amgen Inc. Remote, United States Manager
Same function Same seniority Same country
60%similar
ModernaTX, Inc. Cambridge, United States Manager
Same function Same seniority Same country
60%similar
Servier Boston, United States Manager
Same function Same seniority Same country
50%similar
Lilly Indianapolis, Indiana, United States of America Associate Director
Same function Adjacent seniority Same country
50%similar
Celgene - Summit (Corp) Madison, United States Associate Director
Same function Adjacent seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Global Patient Safety Business Excellence, Senior Manager
Amgen Inc. · Remote, United States · Manager
Function Therapeutic area Seniority Country
60%
Manager, Pharmacovigilance Case Processing (Boston, MA, US)
Servier · Boston, United States · Manager
Function Therapeutic area Seniority Country
50%
Associate Director, PV Scientist
Biogen · Cambridge, United States · Associate Director
Function Therapeutic area Adjacent seniority Country
50%
Associate Director, Epidemiology Strategist
E.R. Squibb & Sons,L.L.C. · Princeton, United States · Associate Director
Function Therapeutic area Adjacent seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.