Patient Safety ICSR Manager
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
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.
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.
Where these roles are based
Top locations among the 38 comparable roles
+ 12 more countries
Seniority mix
38 of 38 peers have a known seniority level
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.
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.
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.