Undergraduate Regulatory Strategist - Oncology
We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.
To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.
Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world.
Undergraduate Regulatory Strategist
Global Regulatory Sciences
Regulatory Strategy
Who can apply?
Applicants must be completing a placement as part of a degree course at a UK University, either through Year in Industry/Industrial Placement or Gap Year.
Please note that we will only consider candidates who have applied by completing the Pfizer Placement Application Form. Candidates who do not complete and attach the application form will NOT be considered.
To learn more about this exciting opportunity, please see below:
Department Overview
* Regulatory Strategy is a dynamic department which proactively partners with drug development and various functional lines to ensure Pfizer meets the requirements of Global Health Authorities.
* Working across all stages of the pharmaceutical product life cycle, Regulatory Strategists aim to secure regulatory approval in a compliant, creative, efficient and commercially viable manner by defining and executing asset-specific regulatory strategies.
* The Regulatory Strategy department leads dialogue with Global Health Authorities on behalf of Pfizer.
* Regulatory Strategy engages with different business functions and regions, offering unique insight to research & development and commercial aspects of the pharmaceutical industry.
What can I achieve and what will I be responsible for whilst completing a placement at Pfizer?
Global Regulatory Sciences supports a diverse portfolio of products spanning three therapeutic areas (Inflammation and Immunology, Vaccines, and Internal medicine, Global Brands and Anti-infectives). You will have the opportunity to develop and implement regulatory strategies for innovative medicinal products and to maintain Pfizer’s marketed products to the highest standards of quality, safety and efficacy, across different regions.
You will be a part of the day to day compilation of general regulatory project documents, clinical trial applications, regulatory dossiers and responses to regulatory questions received from health authorities. You will also contribute to global regulatory strategies and implementation plans, ensuring an aligned regional position is reached and agreed for assigned projects. You will monitor progress of regulatory plans whilst ensuring identified risks are addressed. Moreover, you will take a proactive role in maintaining systems, processes and procedures relating to regulatory strategy.
What other opportunities and benefits do Pfizer offer?
Pfizer has consistently ranked amongst the top 100 graduate employers globally and offers many additional opportunities in the form of:
* Communication and presentation training
* Volunteering opportunities
* Participation in cross-functional projects
* Shadowing opportunities
* Professional membership for The Organization for Professionals in Regulatory Affairs (TOPRA)
* Opportunity to attend the TOPRA Careers Fair
* Flexible working arrangements
* Pfizer Share Ownership Plan
When can I start?
Placements will start 1st September 2025 and will run for 12 months.
PERSON SPECIFICATION
Type of person we are looking for, in relation to ‘Skills’, ‘Knowledge’ and ‘Motivation’:
* Completing placement as part of University Degree either through Year In Industry/Industrial Placement or Gap Year
* Adaptable – Desire to learn and a capacity to assimilate and act on new information quickly
* Analytical – Synthesize complex information and identify potential issues before they arise
* Integrity & Attention to Detail – Appreciate the core function of Regulatory Strategy and work to provide the best outcomes for patients.
* Problem-solving – Use innovative and strategic thinking to develop novel solutions to challenges
* Project management – Ability to manage multiple activities and complete tasks on time.
* Proactive – Self-starter with the ability to work individually and as a team.
* Written & Oral Communication – Ability to convert complex data into succinct messages
* IT Expertise - Proficient in the use of Microsoft Office suite of programmes
This position will close for applications on 17th November 2024.
Please note that we only accept application forms. Please do not send over your CV or cover letter as they will not be considered.
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