You will get Break Into Pharma – 1-on-1 Strategy Session
Project details
This is a focused, 1-on-1 strategy session for anyone trying to start or shift their career in pharma.
You’ll speak directly with me — a senior pharmaceutical physician with 24+ years of experience, including roles as QPPV, Head of Safety, and CMO. I’ve hired, trained, and led teams across clinical development, pharmacovigilance, and regulatory strategy.
We’ll use the time however it’s most helpful to you. That could include:
Choosing between roles in safety, clinical, or regulatory
Deciding what companies or geographies to target
Understanding the real skill gaps (and how to close them)
Feedback on your current approach to CVs or applications
Or just answering all your questions about pharma from the inside
You’ll leave the session with clarity and a shortlist of actions to take next.
You’ll speak directly with me — a senior pharmaceutical physician with 24+ years of experience, including roles as QPPV, Head of Safety, and CMO. I’ve hired, trained, and led teams across clinical development, pharmacovigilance, and regulatory strategy.
We’ll use the time however it’s most helpful to you. That could include:
Choosing between roles in safety, clinical, or regulatory
Deciding what companies or geographies to target
Understanding the real skill gaps (and how to close them)
Feedback on your current approach to CVs or applications
Or just answering all your questions about pharma from the inside
You’ll leave the session with clarity and a shortlist of actions to take next.
Project Type
Business Consulting, Human ResourcesWhat's included $100
These options are included with the project scope.
$100
- Delivery Time 2 days
- Number of Revisions 0
Optional add-ons
You can add these on the next page.
Fast 1 Day Delivery
+$25
CV feedback
+$30
1 review
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ML
Martin Alexander L.
Feb 3, 2026
Pharma/Clinical Expert Needed for Feedback on Trial Summary Tool
Lisa is extremely knowledgeable in everything about clinical drug development and clinical operations. A real star.
About Lisa
Senior Pharmaceutical Physician | Global Safety & Clinical Development
Barcelona, Spain - 11:43 am local time
I now work as a consultant, supporting biotechs, CROs, and health tech companies who need fast, expert-level input without hiring full-time staff. I step in when internal teams need help — whether it’s a signal assessment, an inspection, or a key document that must be ready now.
Why I’m on Upwork:
I’ve built a consulting practice focused on short-term, high-impact support. I’m not between jobs — I’m available on demand for clients who need real expertise and fast answers.
Areas of Expertise:
✔ Safety and benefit–risk strategy
✔ EMA/FDA submissions & regulatory responses
✔ Pharmacovigilance system setup & QPPV support
✔ Inspection readiness and audit rescue
✔ Medical review: protocols, IBs, CSRs, narratives
✔ SOP development (safety, clinical, medical)
✔ Signal detection (incl. EMA ESI) and risk minimization
I also offer one-off strategic calls or document reviews — ideal for early-stage companies or those building their first safety system.
📍 Based in Spain | Available globally | Fast turnaround, clear deliverables, and senior-level clarity
Let’s talk if you need urgent expert support or a reliable partner for a complex challenge.
Steps for completing your project
After purchasing the project, send requirements so Lisa can start the project.
Delivery time starts when Lisa receives requirements from you.
Lisa works on your project following the steps below.
Revisions may occur after the delivery date.
Review materials provided (CV and/or background info)
Conduct a 45-minute video or voice call via Zoom or preferred platform