Video Testimonial
Emeka
Regulatory Medical Writing Graduate
“PharmaLink gave me the vocabulary, the portfolio and the confidence to walk into an industry interview and actually belong there.”
Now in industryYour Healthcare Career Prepared You for This. We Prepare You for What’s Next.
Practical programmes in Regulatory Medical Writing and Pharmacovigilance. Industry-delivered, anchored to real deliverables, led by people who have lived the work.
430+Graduates
69%Placement Rate
LiveExpert Teaching
2Cohorts / Month
Hear From Our Graduates
Real People. Real Pharma Careers.
Graduates of PharmaLink Academy talk about what changed — unscripted, on camera.
Video Testimonial
Sasu
Regulatory Medical Writing Graduate
“I stopped applying blind. PharmaLink showed me what pharma hiring managers actually look for — and how to show up as that person.”
Now in industry
Video Testimonial
Joannita
Regulatory Medical Writing Graduate
“The scenarios, the expert panels, the real feedback — it wasn’t a course, it was rehearsal for the job I now have.”
Now in industry
Video Testimonial
Katie
Physician Associate — Pharma Transition
“Clinical practice taught me the science. PharmaLink taught me how pharma actually hires, speaks and builds careers — and got me through the door.”
Clinical → Industry“PharmaLink gave me the vocabulary, the portfolio and the confidence to walk into a pharma interview and actually belong there.”
“I stopped applying blind. PharmaLink showed me what hiring managers actually look for — and how to show up as that person.”
“Clinical practice taught me the science. PharmaLink taught me how pharma actually hires — and got me through the door.”
The PharmaLink Moat
Two things you won’t find in any other pharma programme
FORGE™ and VIGILANT™ are the reason our graduates arrive day-one productive — not day-ninety trainable. One is a live industry environment. The other is a proprietary method. Together they are why hiring managers keep coming back.
FORGE™ · Live Simulator
Walk into the meetings before you walk into the job
FORGE™ drops writers into a running pharmaceutical programme — cross-functional meetings in session, regulators firing queries, timelines shifting, parallel deliverables in flight. The same pressure a sponsor-side regulatory writer faces on any given day.
Scenario in progress
“You’re the lead writer on a Phase III oncology programme, day 47. MHRA has come back with 14 protocol queries. Biostats just flagged an efficacy signal. Your PM wants the briefing book on her desk by Friday.”
- →Live cross-functional meetings with sponsor PM, regulatory affairs, biostats and clinical lead roles
- →Real-time scenario events — regulatory queries, protocol amendments, safety signals, timeline shifts
- →Stakeholder inbox and decision queue under competing priorities
- →Parallel deliverables on a project board, not a single document
£1,999 add-on · pairs with RMW or runs standalone
FORGE™ · Launching 1 May 2026
VIGILANT™ · PV Method
The method behind every PV graduate we place
VIGILANT™ is our proprietary pharmacovigilance method — the structured path from an ICSR arriving in the inbox to inspection-ready evidence on the shelf. It’s what turns drug safety knowledge into drug safety judgment.
Method in practice
“Valid case or not? Serious or not? Expected or not? Signal or noise? The answers change who does what next — VIGILANT™ gives you the framework to call it under pressure and back the call with evidence.”
- →ICSR intake and triage discipline — validity, seriousness, expectedness, causality
- →Narrative writing and MedDRA coding calibrated to regulator expectations
- →Signal-to-decision flow — detection, assessment, regulatory action, documentation
- →Inspection-ready quality trails built for MHRA, EMA and FDA scrutiny
Inside Tier 1 £1,799 and Tier 1 & 2 £3,999
Explore PV Programme
Every graduate leaves with FORGE™ reps under their belt or the VIGILANT™ method in their pocket — the difference between a certificate on the wall and a hire on the desk.
Who This Is For
Built for healthcare and life science professionals ready to move into industry
Our programmes meet three kinds of candidates where they are today — and move them into the regulatory, drug safety and medical writing roles industry is hiring for.
Rx
Clinical & Hospital Pharmacists
Today
Protocol-led dispensing and clinical practice, limited visibility into the regulatory and safety work that sits upstream of the medicines you handle.
After PharmaLink
Drug safety, pharmacovigilance and regulatory medical writing roles that pay for the clinical judgement you already have.
MSc
Life Science Graduates (MSc / PhD)
Today
Strong scientific training, but locked out of industry because academic writing and bench research don’t translate to regulated pharma deliverables.
After PharmaLink
An industry-ready portfolio of regulatory documents, PV case narratives and protocols — the evidence recruiters and hiring managers actually look for.
MD
Medical Doctors & Allied Health
Today
Patient-facing clinical work, considering a pivot to industry but without a clear route into drug safety, medical affairs or medical writing.
After PharmaLink
Pharmacovigilance, medical writing and medical affairs positions where clinical insight translates directly into industry-grade output.
Book a Discovery Call
15-minute call · see which programme fits your background
Programmes & Investment
Pick the programme that matches the role you’re going after
Transparent pricing. Two cohorts a month. Career support and job-search coaching included in every programme — the FORGE™ live simulator is an optional add-on to RMW.
RMW
Regulatory & Medical Writing Programme
For pharmacists, life-science grads and MDs moving into regulatory writing, medical writing or clinical documentation.
£2,999
per cohort · 2 cohorts/month
- ✓ Protocols, CSRs, briefing books
- ✓ Regulatory writing framework
- ✓ Industry mentor feedback loops
- ✓ Career support & job-search coaching
FORGE™ · Add-on
FORGE™ Live Simulator
Standalone live scenario simulator. Practise real industry meetings, stakeholder queries and parallel deliverables under time pressure. Add on to RMW or run it alongside.
£1,999
add-on · pair with RMW
- ✓ Live industry meeting simulations
- ✓ Stakeholder queries under pressure
- ✓ Parallel deliverables workflow
- ✓ Pair with RMW or run standalone
PV · Tier 1
Pharmacovigilance — Case Processing Foundations
Entry point into drug safety: ICSR intake, triage, narrative writing and MedDRA coding under the VIGILANT™ method.
£1,799
per cohort · 2 cohorts/month
- ✓ ICSR intake & triage workflows
- ✓ Narrative writing & MedDRA coding
- ✓ VIGILANT™ method training
- ✓ Career support & job-search coaching
Most Complete
PV · Tier 1 & 2
Pharmacovigilance — Full Tier 1 & 2
Everything in Tier 1, plus signal management, aggregate reporting and inspection readiness — the end-to-end PV pathway industry hires for.
£3,999
per cohort · 2 cohorts/month
- ✓ Everything in Tier 1
- ✓ Signal management & detection
- ✓ Aggregate reporting (PBRER, DSUR)
- ✓ Inspection readiness & QMS
Not sure which programme fits? Book a 20-minute call and we’ll map it to your target role.
Book a Discovery CallMeet the Founder
Built by Someone Who’s Been Where You Want to Go
18+ years in pharma · RMW & PVPharmaLink Academy was founded by Dorothy Ogwuru, a pharmaceutical professional with over 18 years of experience across regulatory medical writing and pharmacovigilance.
Dorothy began her career in clinical data management immediately after graduating, then joined Novartis as a pharmacovigilance associate within months. Over seven years, she progressed to Global Pharmacovigilance Head level before transitioning into full-time regulatory medical writing in 2015. She has worked with multiple global pharmaceutical companies, built consulting income streams, and mentored dozens of individuals into pharma roles.
PharmaLink Academy was born from a simple observation: brilliant healthcare professionals were being held back not by lack of talent, but by lack of exposure to how the pharmaceutical industry actually operates. The programmes are designed to close that gap — because Dorothy has lived on both sides of it.
Dorothy Ogwuru
Founder, PharmaLink Academy
Read Dorothy’s Full Story →Industry Engagement
Recognised Across the Industry
PharmaLink Academy contributes to professional, academic and industry conversations focused on developing industry-ready pharmaceutical professionals. Through university engagement, industry events and sector discussions, we support greater understanding of pharmaceutical career pathways and workforce development across the life sciences ecosystem.
Spoken at & featured atSelected industry engagements
The Pharmacy Show
University of Leicester
OSCEs & Beyond
UK Pharmacy Schools
Where PharmaLink Academy Alumni Work Today
Logos represent organisations PharmaLink academy alumni are currently employed. Logos are displayed for informational purposes only and do not imply partnership or endorsement.
Frequently Asked Questions
Straight Answers Before You Enrol
The ten questions prospective students ask most often. Still unsure? Book a 15-minute call with the team.
Do I need prior pharmaceutical industry experience to enrol?
No. PharmaLink Academy was designed specifically for healthcare professionals, life-science graduates and career-transitioners who have no prior pharma industry experience. You bring your clinical or scientific background; we build the regulatory, safety and documentation skills the industry actually requires.
How long are the programmes and how much time do I need each week?
Regulatory Medical Writing (RMW) is a 6-month structured pathway. Pharmacovigilance (PV) is flexible: Tier 1 typically completes in 3–4 months and the full Tier 1 & 2 programme in 6–7 months.
Plan for 6–10 hours per week on average across assignments, live expert sessions and portfolio work. The programmes are designed to fit around full-time employment.
What is FORGE™ and do I need it?
FORGE™ is our live scenario simulator. It puts you inside 19 real industry situations across five themes — regulatory authority pressure, cross-functional tension, operational reality, PV-specific challenges, and interpersonal pressure — guided by experts who have lived every one.
FORGE™ is an optional £1,999 add-on, not bundled into RMW or PV. Most students take it when they want full rehearsal of the hiring gauntlet before interviews begin; others add it later once they see the gap.
What is VIGILANT™ and who gets access?
VIGILANT™ is our proprietary simulated pharmacovigilance safety database, built from scratch to replicate the workflows used inside real pharma safety departments — ICSR entry, MedDRA coding, narrative writing, aggregate reporting and signal detection.
VIGILANT™ is included with the Pharmacovigilance programme (both Tier 1 and Full). No other UK training provider offers a live PV database simulator of this depth.
What’s the difference between PV Tier 1 and PV Full (Tier 1 & 2)?
PV Tier 1 (£1,799) covers case-processing foundations: ICSRs, narrative writing, MedDRA coding and reporting timelines — everything you need for your first PV operations role.
PV Full, Tier 1 & 2 (£3,999) adds signal management, aggregate reporting (PSURs, PBRERs, DSURs), inspection readiness and senior-level PV decision-making — the full path into mid-career PV roles.
Can I pay in instalments?
Yes. Every programme offers flexible payment plans alongside the upfront price. Instalment options and amounts are shown on each programme page — book a 15-minute call and we’ll walk you through the plan that fits your situation.
Are the programmes CPD accredited?
Yes. PharmaLink Academy programmes are CPD accredited, and completion contributes formally to your continuing professional development record.
Do you place me directly into a pharma role?
We don’t make direct placements — and we are careful not to claim we do. What we offer is career support and job-search coaching: CV and LinkedIn review, interview rehearsal (including the FORGE™ scenario lab), employer exposure through expert panels, and ongoing mentoring into your first role.
The outcome our graduates consistently report: they walk into interviews ready, and hiring managers recognise them as industry-ready rather than “still learning.”
When does the next cohort start?
RMW runs two cohorts per month — you can start within weeks of enrolment. PV cohorts run monthly. Exact next-start dates are shown on each programme page and confirmed during your booking call.
What if I’m not sure which programme is right for me?
Book a free 15-minute strategy call. We’ll look at your background, your target pharma role and your timeline, and tell you honestly whether RMW, PV, PV Full, or the FORGE™ add-on is the right fit — or whether PharmaLink isn’t the right answer for you at all.
Begin Your Pharmaceutical Industry Transition With Confidence
PharmaLink Academy supports professionals ready to move into pharmaceutical environments through structured capability development grounded in real‑world practice.
