NoxPharm helps tailor your CV to the language of each role — ICH guidelines, GVP modules, MedDRA, CTD, the lot — so your experience is easier to understand.
Pharma · Biotech · CRO · Medical Devices · Life Sciences
Free to start · No credit card required · 3 tailored applications/month on Free plan
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Job Match Score
ATS Keywords
Tailored CV
AI-OptimisedSARAH MITCHELL
Drug Safety Scientist · Basel, CH · s.mitchell@email.com
Professional Summary
Pharmacovigilance specialist with 8+ years in ICH E2C Safety Reporting and PSUR/PBRER authoring across EU MAH submissions.
Experience
Drug Safety Scientist II · Novartis · 2020–Present
Led signal detection using ARGUS/ARISg, authored MedDRA v26 case series across 4 TAs.
PV Associate · Parexel · 2018–2020
Processed ICSRs, maintained PSMF documentation for 3 MAH clients.
Core Skills
Skill Gap Analysis
ActiveIntelligence Suite
Before & After
One upload. Your existing experience reframed around the language and requirements in the job description.
Responsible for safety reporting
Supported regulatory submissions
Involved in clinical data review
Helped with audit preparation
Managed ICSR processing and safety reporting in compliance with EMA & FDA pharmacovigilance requirements
Led EU CTD regulatory submissions across 3 NDA dossiers submitted to EMA
Reviewed clinical datasets per ICH E6 GCP across 12 investigational sites
Coordinated GxP audit programme — CAPA closure rate 98% within 30 days
Designed for professionals at
How it works
Paste the JD. Upload your CV. Get a tailored application package — match score, cover letter, and all.
Paste the job description text or a supported job URL. NoxPharm extracts the role requirements and separates must-have signals from nice-to-have ones.
Upload your PDF or DOCX. We parse your full history — experience, skills, certifications, regulatory background — and map it against the role.
Most application packages are generated in about a minute; larger CVs or longer job descriptions may take a little longer.
Most CV tools don't know the difference between a PSUR and a PBRER. We do.
We align your CV with the terminology and requirements in the job description, without keyword stuffing.
ICH guidelines, GVP modules, MedDRA, CTD, PSUR, IMPD. We don't need you to explain what these are.
Each application is written for one role, one team, one hiring manager. Not a template with your name swapped in.
Turn a time-consuming manual rewrite into a faster, more focused tailoring workflow.
8
Life sciences specialisms
Thousands
Life-sciences roles
About 1m
Typical package generation
50+
Supported role families
Pricing
Start free. No commitment. Upgrade when you're ready for the full suite.
3 tailored applications/month — no credit card needed.
No daily cap. Tailor up to 50 applications per month with the full CV engine.
Full career intelligence. Interview prep, salary data, premium templates.
What's included
From finding the right job to tailoring your CV and prepping for the interview. All built for life sciences. All speaking your language.
Your CV should make specialist experience easy to understand. NoxPharm helps translate it into the terminology and requirements used in the job description.
NoxPharm helps align your CV with the terminology and requirements in the job description, so recruiters and screening tools can understand your fit more quickly.
Know exactly where you stand before you apply. Every must-have and nice-to-have requirement mapped to your experience — with a clear path for each gap.
Not generic prompts. Scenario-based questions built from the exact JD you applied for — the kind a Senior Drug Safety Scientist at Roche would actually get asked.
See how your CV may read to a recruiter: strengths, unclear points, and gaps worth closing before you apply.
Most people leave money on the table by naming a number first. Market-rate benchmarks for your role, location, and seniority — and a script so you don't have to wing it.
Stop losing track of what you sent where. Keep each application status in one view, linked to your tailored CV and match score.
Drop in a job description and NoxPharm classifies the role family — PV, RA, Clinical, MSL, QA, HEOR. No dropdowns. No manual setup.
Browse live pharma, biotech, CRO, medtech, and life-sciences roles refreshed regularly from employer career sites and ATS-hosted career pages.
No CV? No problem. Students and graduates fill in a short form — education, thesis, skills, target role — and get a pharma-native, ATS-friendly CV.
We built a pharma-only job board directly inside NoxPharm. Browse live pharma, biotech, CRO, medtech, and life-sciences roles refreshed regularly from employer career sites and ATS-hosted career pages.
Drug Safety Scientist II
88%
match
Senior CRA — Phase II/III
74%
match
Regulatory Affairs Manager
61%
match
Jobs For You
AI-matched · Pro plan
Just finishing your MSc or PhD in Pharma, Life Sciences, or Biotech? Our AI turns your education, lab work, and thesis into a professional, ATS-friendly CV — no blank page, no guessing.
Personal Details
Name, email, location, LinkedIn
Education
Degree, institution, thesis, modules
Experience & Skills
Internships, lab work, tools, languages
Target Role
Desired position & sector — AI does the rest
Your CV is ready.
Tailored. ATS-friendly. Pharma-native.
The NoxPharm extension detects pharma jobs on LinkedIn, Indeed, Glassdoor and more. One click sends the full job description to NoxPharm — no copy-pasting.
Regulatory Affairs Specialist — Novartis
Dublin, Ireland
Where we work
Big Pharma, biotech, CRO, medical devices — we optimise for role-specific terminology, competency language, and job-description requirements.
Big Pharma
Roche, Novartis, Pfizer, AZ
Optimised for Big Pharma terminology and competency frameworks
Biotech
Clinical-stage & commercial
Built for fast-moving biotech environments across all functions
CROs
ICON, Parexel, Covance, Syneos
CRO-specific roles from CRA to CTM to QA Manager
Medical Devices
Medtech, diagnostics, IVD
Covers MDR/IVDR regulatory and medtech role families
Clinical Research
Phase I – IV globally
Deep expertise in trial operations, sites, and data roles
Pharmacovigilance
PV hubs & signal management
Full PV coverage from Associate to QPPV across MAH and CRO
Healthcare Data
RWE, HEOR, Health Economics
Specialist coverage for outcomes research and payer access
Generics & Biosimilars
Regulatory & quality
Regulatory and QA in generics, biosimilar, and API manufacturers
Your role. Your language.
From Drug Safety Associate to QPPV. CRA to Clinical Operations Manager. Medical Writer to Global Medical Director. We know the roles, the language, and what good looks like.
FAQ
Questions we get asked most — and honest answers to each.
Paste a job description. Upload your CV. Get a tailored application package in about a minute. No credit card. No onboarding call. No generic output.
No credit card required · 3 tailored applications/month free · Cancel anytime