PharmaLink Academy
Senior PV Expert – Instructor
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PharmaLink Academy
PharmaLink Academy is a specialised training academy focused on helping healthcare and life sciences professionals transition into careers within the pharmaceutical industry. Through structured, instructor-led programs, practical assignments, and expert mentorship, the academy equips students with the real-world knowledge and regulatory understanding needed to succeed in areas such as Regulatory Medical Writing and Pharmacovigilance.
Important Note (Please Read Before Applying)
This role is designed for professionals with hands-on, end-to-end pharmacovigilance experience within pharmaceutical companies, CROs, or PV consulting environments.
We are specifically seeking professionals who have worked across the full PV lifecycle, not specialists confined to a single function.
Role Overview
This position combines pharmacovigilance expertise with training and mentorship.
You will deliver structured live sessions explaining PV frameworks and processes, review student assignments, and provide career guidance to professionals entering or transitioning into pharmacovigilance.
The role is remote and full-time, based in the UK or EU, designed for experienced PV professionals who want to train and shape the next generation of talent at scale.
Key Responsibilities
- Deliver Pharmacovigilance Training
- Conduct live training sessions covering the full PV lifecycle: case intake, triage, medical review, MedDRA coding, causality assessment, signal detection, and risk management
- Teach key frameworks including GVP modules, ICH E2 series, and expedited/periodic reporting requirements
- Break down complex PV processes in a clear and structured way for students
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Assignment Review & Feedback
- Review student assignments related to pharmacovigilance case handling and reporting
- Provide detailed, structured feedback aligned to industry and regulatory standards
- Evaluate assignments based on GVP and ICH compliance expectations
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Student Mentorship & Career Support
- Guide students with CV preparation, interview readiness, and job search strategy
- Help students understand career pathways within pharmacovigilance
- Provide professional guidance and encouragement during the transition into industry roles
Typical PV Areas You Should Have Experience With
Ideal candidates will have hands-on experience across:
- Case Processing & Triage
- Medical Review & Causality Assessment
- MedDRA Coding
- Signal Detection & Risk Management
- PSURs/PBRERs and DSURs
- Expedited Reporting (e.g., SUSARs) and Regulatory Submissions
Ideal Candidate Profile
We are seeking experienced PV professionals who combine end-to-end technical expertise with strong communication and mentoring ability.
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Requirements:
- Minimum Life Sciences degree (Pharmacy, Biotechnology, Life Sciences, or related field)
- 10+ years of experience in Pharmacovigilance, with genuine end-to-end exposure
- Experience working in pharmaceutical companies, CROs, or regulatory consulting environments
- Strong understanding of GVP modules and ICH guidelines
- Comfortable delivering live teaching or training sessions to large groups
- Strong written communication and feedback skills
- Interest in mentoring professionals entering the pharmaceutical industry
- UK or EU-based
Ideal candidates may currently work as:
- Senior PV Specialist
- Pharmacovigilance Manager
- Drug Safety Physician
- Senior Safety Scientist
- Principal PV Associate
Working Hours
Full time - Remote
Live sessions delivered at:
6:00 p.m. BST
Candidates must be comfortable presenting at this time.
Why Join PharmaLink Academy
- Work with professionals transitioning into the pharmaceutical industry
- Share your regulatory expertise and shape future Pharmacovigilance associates
- Flexible remote part-time structure
- Opportunity to create long-term impact through training and mentorship
How to Apply
Interested candidates should send CV and portfolio to voke@pharmalinkacademy.co.uk highlighting:
- PV experience
- Pharmaceutical or CRO background
- Experience with PV documentations
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