Launch yourcareerinlife sciences.

Live cohorts in Pharmacovigilance, Regulatory Affairs, Clinical Research, and Clinical Data Management — paired with a job board, resume tools, and interview prep for the Canadian market.

Daniel K.Priya S.

Recent placements

Mississauga · Toronto

Next batch June 3, 2026Format Live · 30 days

Graduates placed at

  • IQVIA
  • Bayer
  • GSK
  • Veristat
  • Syneos Health
  • PPD
  • Health Canada
  • AstraZeneca
  • Novartis
  • Sanofi
  • Pfizer
  • Apotex
  • IQVIA
  • Bayer
  • GSK
  • Veristat
  • Syneos Health
  • PPD
  • Health Canada
  • AstraZeneca
  • Novartis
  • Sanofi
  • Pfizer
  • Apotex

Four tracks

Each program is eight weeks of live instruction, hands-on labs, and 1:1 reviews. Pick one — or stack multiple at a discount.

Patient safety, end to end

Pharmacovigilance

Case processing, signal detection, periodic reporting, and regulatory submissions across FDA, Health Canada, and EMA.

View program

Become a clinical trial specialist

Clinical Research

Learn ICH-GCP, study design, monitoring, and the trial lifecycle from protocol to closeout — guided by a Canada-based clinical lead.

View program

Own the data behind every trial

Clinical Data Management

Master EDC systems, CRF design, query management, and CDISC standards — the operational backbone of every modern trial.

View program

Bring therapies to market

Regulatory Affairs

Submission strategy, eCTD authoring, and life-cycle management across Health Canada, FDA, and EMA — built for the Canadian market.

View program

— Why Avenir

Built for the gap between graduation and your first regulated role.

A job board tagged to your track

Only roles relevant to courses you own — no PV listings in your CDM feed.

Resume that recruiters open

ATS-friendly templates designed for RA, PV, CR, and CDM. Live preview.

Interview prep that mirrors real screens

Curated banks for ICH-GCP, Health Canada, FDA, EMA — with sample answers.

A Kanban tracker for every application

Move cards Applied → Interview → Offer → Rejected. Stay organized.

Certified completion

Verifiable certificate on completion. Upload it directly to LinkedIn.

WhatsApp office hours

Ask the team anything before, during, and after the program. Real reply within hours.

Meet your instructor

From the field.

Gopal Chelikani

Gopal Chelikani

Study Coordinator @ Amgen · Clinical Operations & Regulatory Affairs

Has spent the last decade inside global pharma and CROs — coordinating clinical trial execution, owning eCTD lifecycle submissions to Health Canada and the FDA, and managing Trial Master Files for oncology and imaging studies. Today he leads study coordination at Amgen in Toronto. Every Avenir cohort is taught with real anonymised case studies, the same templates he has used in regulated submissions at Amgen, WorldCare, Hetero and Parexel — plus weekly 1:1 office hours so no student gets stuck.

Years
12+
Based in
Toronto
Specialization
eCTD lifecycle lead — Health Canada, FDA (NDS, SNDS, IND, NDA, BLA)

EducationMSc Regulatory Affairs (Clinical Research) · Northeastern University

Worked acrossAmgenPulseBridgeWorldCareImaging EndpointsHeteroParexel

— Stories

“The case-processing labs felt like real day-1 work. My first week on the job was just continuation of class.”
Daniel K.

Daniel K.

PV Associate — IQVIA, Mississauga

““The instructor walked us through real eCTD structures. That clarity made the difference in interviews.””
Priya S.

Priya S.

RA Specialist — Bayer, Toronto

— Ready when you are

Apply in two minutes.
We reply within twenty-four hours.

No payment on this site. Our admissions team handles billing off-platform once your application is reviewed.

Apply nowTalk to us