PharmacovigilanceRegulatory AffairsClinical ResearchMedical AffairsQA & GxPMedical Writing+ 2 more

Your experience is strong. Your CV needs to prove it.

NoxPharm tailors your CV to the exact language of each role — ICH guidelines, GVP modules, MedDRA, CTD, the lot — so your application actually gets read.

Pharma  ·  Biotech  ·  CRO  ·  Medical Devices  ·  Life Sciences

Free to start · No credit card required · 3 CVs/day on Free plan

2,400+ CVs tailoredResults in under 60sNo credit card

Live workspace preview

noxpharm.com/dashboard
NoxPharm/Senior Drug Safety Scientist
Analysis complete
Match Score
Skill Gap
Tailored CV
Cover Letter
Interview Prep
Recruiter Insights
Salary Guidance

Job Match Score

88/ 100
Must-have coverage91%
Nice-to-have fit78%
ATS optimisation94%

ATS Keywords

Pharmacovigilance ICH E2C MedDRA v26 PSUR/PBRER Signal Detection XEVMPD Veeva Vault ARGUS/ARISg

Tailored CV

AI-Optimised

SARAH 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

ICH E2C/E2EPSUR/PBRERSignal DetectionMedDRAGVP ModulesARGUS
Page 1 of 212 keywords matched

Skill Gap Analysis

Active
ICH E2E & PSMF experience
MedDRA coding (v26+)
Signal detection tools
PSUR/PBRER authoring
!XEVMPD/IDMP submissions
!Veeva Vault SafetyDocs

Intelligence Suite

Tailored CVReady
Cover LetterReady
ATS VersionReady
Interview PrepPro
Recruiter InsightsPro
Salary GuidancePro
Export CV
Track App

Before & After

Same experience. Different results.

One upload. Your existing experience reframed in the exact language the hiring team used in their JD.

Before

Responsible for safety reporting

Supported regulatory submissions

Involved in clinical data review

Helped with audit preparation

Match Score
29%
After NoxPharm

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

Match Score
87%

Designed for professionals at

Big PharmaBiotechCROsMedical DevicesDiagnosticsClinical ResearchPV HubsGenerics & Biosimilars

Your CV speaks pharma. So does NoxPharm.

Most CV tools don't know the difference between a PSUR and a PBRER. We do.

ATS-aligned from the start

ATS systems filter before a human reads your name. We align your keywords to exactly what they're scanning for — not guesswork.

Speaks your language

ICH guidelines, GVP modules, MedDRA, CTD, PSUR, IMPD. We don't need you to explain what these are.

One JD. One CV.

Each application is written for one role, one team, one hiring manager. Not a template with your name swapped in.

Save hours per application

What takes 3+ hours by hand takes under 5 minutes. Apply to more roles, with a stronger CV each time.

In their words

What happened when they stopped guessing

Featured
I'd been applying to PV roles for four months with no response. NoxPharm showed me I was hitting 28% of the must-have keywords. After one rewrite, I had three callbacks in a week — including one from Novartis Basel I'd already applied to twice before.
LB

Lukas B.

Drug Safety Scientist → Senior PV Specialist

Novartis · Basel

Verified
I went from spending 3 hours tailoring each CV to under 5 minutes. The skill gap analysis showed me exactly which regulatory modules to highlight for EU affiliate roles. Got two interviews in the first week.
SM

Sarah M.

Senior Pharmacovigilance Specialist

Global CRO · Zurich

Verified
The ATS optimisation alone is worth it. I was applying to Big Pharma roles for months with no callbacks. NoxPharm showed me I was missing 12 of their exact keywords. One rewrite later — shortlisted.
JK

James K.

Regulatory Affairs Manager

Biotech · Basel

Verified
Interview prep is genuinely excellent for MSL roles. The questions were scenario-based and aligned to the actual JD. It felt like practising with someone who knew exactly what the hiring team would ask.
PR

Dr. Priya R.

Medical Science Liaison

Top-10 Pharma · London

Verified
Moving from clinical research into Medical Writing felt like starting over. NoxPharm mapped exactly which of my GCP and protocol experience was transferable — and rewrote my CV to lead with it. First interview within 10 days.
AL

Anna L.

CRA → Medical Writer

CRO · Manchester

TrustpilotSee our profile

We're building trust with Life Sciences professionals. Share your experience on Trustpilot.

GDPR CompliantEncrypted & SecureFiles auto-deletedNo card to try free

2,400+

CVs tailored

8

Life sciences specialisms

<60s

Average turnaround

4.8/5

User satisfaction

How it works

Three steps. Under 60 seconds.

Paste the JD. Upload your CV. Get a tailored application package — match score, cover letter, and all.

01

Paste the Job Description

Paste the JD text or a LinkedIn/Indeed URL. We read every requirement and classify each one as must-have or nice-to-have — the way a hiring manager actually thinks.

02

Upload Your CV

Upload your PDF or DOCX. We parse your full history — experience, skills, certifications, regulatory background — and map it against the role.

03

Get Your Application Package

Your tailored CV, match score, and cover letter are ready in under 60 seconds. Interview prep, recruiter insights, and salary guidance follow — same workspace.

What's included

Eight tools. One workspace.

From tailoring your CV to prepping for the interview. All built for life sciences. All speaking your language.

CV Tailoring

Your CV shouldn't need to explain what an ICSR is. NoxPharm rewrites it to use the exact phrasing the hiring team put in the JD — not a template, not a generic pass.

ATS Optimisation

Most applications don't get rejected. They never get seen. We align your keywords to exactly what the ATS is scanning for — before a human reads your name.

Skill Gap Analysis

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.

Interview Preparation

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.

Recruiter Insights

The recruiter reviewing your CV spent 11 seconds on it. Here's what they saw — your perceived strengths, the red flags they'd raise, and the gaps worth closing.

Salary Intelligence

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.

Application Tracker

Stop losing track of what you sent where. Every application — saved to shortlisted to offer — in one view, linked to your tailored CV and match score.

Auto Role Detection

Drop in a job description and we'll tell you exactly what we're dealing with — PV, RA, Clinical, MSL, QA, HEOR. No dropdowns. No manual setup.

Where we work

Wherever you are in life sciences, your role is covered.

Big Pharma, biotech, CRO, medical devices — we optimise for the specific ATS, competency language, and hiring patterns of each.

Big Pharma

Roche, Novartis, Pfizer, AZ

Optimised for Big Pharma ATS patterns 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.

Every major life sciences role, fully understood.

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.

Pharmacovigilance & Drug Safety

  • Drug Safety Associate
  • PV Scientist
  • Signal Detection Manager
  • QPPV & Deputy QPPV
  • Safety Medical Reviewer
  • Aggregate Report Writer

Regulatory Affairs

  • Regulatory Affairs Associate
  • RA Manager & Director
  • CMC Regulatory Lead
  • Regulatory Submissions Manager
  • EU/US RA Specialist
  • Labelling & Artwork Manager

Clinical Operations

  • Clinical Research Associate (CRA)
  • Clinical Trial Manager (CTM)
  • Clinical Operations Manager
  • Clinical Trial Coordinator
  • Site Activation Manager
  • Study Start-Up Specialist

Medical Affairs & MSL

  • Medical Science Liaison (MSL)
  • Medical Advisor
  • Global Medical Director
  • Field Medical Director
  • Medical Education Manager
  • Scientific Communications Lead

Medical Writing

  • Medical Writer
  • Senior Medical Writer
  • Regulatory Medical Writer
  • Publication Manager
  • Clinical Study Report Writer
  • Scientific Writer

QA & GxP Compliance

  • QA Specialist
  • QA Manager
  • GxP Auditor
  • CAPA Manager
  • Quality Systems Lead
  • Validation Specialist

Market Access & HEOR

  • HEOR Analyst
  • Health Economist
  • Market Access Manager
  • Outcomes Research Scientist
  • Payer Strategy Lead
  • Value & Evidence Director

Commercial & Strategy

  • Commercial Operations Manager
  • Key Account Manager — Pharma
  • Business Development Manager
  • Brand Manager — Rx Products
  • Strategic Planning Analyst
  • Portfolio Strategy Lead

Pricing

Simple, transparent pricing

Start free. No commitment. Upgrade when you're ready for the full suite.

Free

€0/month

Try the full engine. 3 tailored CVs per day, no card needed.

  • Tailored CV per job description
  • Must-have/nice-to-have gap analysis
  • Match score with section breakdown
  • Cover letter generation
  • ATS keyword optimisation
  • PDF & DOCX export
Start Free
Most Popular

Starter

€19/month

No daily cap. Apply to every role you want — full engine, no limit.

  • Everything in Free
  • No daily project limit
  • Skill gap analysis
  • Job application tracker
Start Starter

Pro

€29/month

The full suite. Interview prep, salary guidance, and premium CV templates.

  • Everything in Starter
  • Interview preparation
  • Recruiter insights
  • Salary guidance & negotiation script
  • Premium CV templates
Start Pro

FAQ

Straight answers

Questions we get asked most — and honest answers to each.

Which Life Sciences roles does NoxPharm support?
Eight role families: Pharmacovigilance & Drug Safety, Regulatory Affairs, Clinical Operations (CRA, CTM, Biostatistics), Medical & Scientific Strategy (MSL, Medical Advisor), Medical Writing, QA & GxP Compliance, Market Access & HEOR, and Commercial & Strategy. Drop in a JD and the system classifies it automatically — no dropdowns, no setup.
Does NoxPharm work for global pharma companies like Roche, Novartis, or Pfizer?
Yes — and it matters that we know the difference between them. Roche, Novartis, AstraZeneca, Pfizer, J&J, Sanofi — they all use different ATS systems, different competency frameworks, and different language in their JDs. We've built for that. Same goes for CROs like ICON, Parexel, and Syneos. The optimisation is specific, not generic.
Is NoxPharm an ATS simulator?
No — and that's intentional. Rather than giving you a black-box score, we show you exactly what's happening. Every JD requirement is classified as must-have or nice-to-have, and we map your CV against each one directly. You see exactly where the gaps are — and what to do about them.
How is my personal data and CV protected?
Your raw CV file is deleted immediately after we extract the text. We only retain what we need to generate your output. We never train AI models on your personal data. The platform is fully GDPR-compliant, and your information is never shared with employers, recruiters, or third parties — ever.
I'm transitioning between pharma roles — can NoxPharm help?
This is honestly where NoxPharm is most useful. The skill gap analysis shows which of your existing experience transfers directly, which you need to frame differently, and which gaps are real. We don't just rewrite your CV — we tell you the truth about the match, and show you how to close it. Whether you're going from CRA to CTM, PV Associate to Safety Scientist, or crossing into Medical Affairs, the system maps your history to the target role honestly.
Can I cancel my subscription at any time?
Yes. No lock-in, no cancellation fees. Cancel Starter or Pro any time from your account settings or billing portal. You stay on your current plan until the billing period ends, and you won't be charged again.
How quickly do I get results?
Your tailored CV, match score, and cover letter are ready in under 60 seconds. Skill gap analysis, interview prep questions, recruiter insights, and salary guidance all generate in the same workspace — typically within 2–3 minutes of uploading your CV.
NoxPharm

Your next role is out there. Your CV just needs to catch up.

Paste a job description. Upload your CV. Get a tailored application in under 60 seconds. No credit card. No onboarding call. No generic output.

Try for free

No credit card required · 3 CVs/day free · Cancel anytime