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Planet Pharma

Associate Director, Global Regulatory Strategy

Hertfordshire
Posted about 17 hours ago
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Unlock Your Potential as an Associate Director, Global Regulatory Strategy

Are you a strategic thinker with a passion for shaping global regulatory pathways in the pharmaceutical industry? Join a dynamic team at the forefront of neurology and beyond, where your expertise will drive impactful regulatory strategies across international markets. This role offers the opportunity to collaborate with senior stakeholders, influence industry initiatives, and lead initiatives across a range of neurological indications, including insomnia, narcolepsy, and epilepsy. If you’re ready to make a meaningful difference in a fast-paced environment and bring innovative ideas to life, this is your chance to thrive in a pivotal leadership position.

Required Skills

  • Exceptional communication skills, both written and verbal, demonstrated through clear, impactful responses and comprehensive coverage sheets
  • Proven experience in development and/or established product regulatory processes
  • Experience leading health authority meetings, particularly with EMA or other global agencies
  • Strong understanding of MAA and CTA processes
  • Ability to work independently and provide strategic input within a collaborative team setting
  • Flexibility to engage with international regulatory activities and a variety of product indications
  • Demonstrated responsiveness and agility in communication and issue resolution

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PwC·London, UK
£35,000/yr

Why you're a good match

Strong

Your economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.

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Why you're a good match

You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.

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Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.

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Nice to Have Skills

  • Background in neurology or specialty therapeutic areas
  • Experience working on US or Rest of World regulatory strategies
  • Proven track record of representing organizations at industry conferences and initiatives
  • Familiarity with CMC and labeling considerations (though not a primary focus)
  • Exposure to cross-functional collaboration spanning clinical development and regulatory affairs

Preferred Education And Experience

  • Bachelor’s degree in Life Sciences, Pharmacy, or related discipline; Advanced degree preferred
  • Minimum of 8+ years in regulatory affairs, with leadership experience in global or regional teams
  • Demonstrated success in leading regulatory submissions and interactions with health authorities
  • Prior involvement in neurology or related therapeutic areas is advantageous

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Other Requirements

  • Ability to work in a hybrid environment, with approximately 3 days per week on-site
  • Willingness to engage in industry initiatives and represent the organization at conferences
  • Proactive approach to stakeholder engagement and strategic planning
  • Eligibility to work internationally and travel as needed for global meetings and conferences

Take the next step in your regulatory career and become a key driver of innovation and leadership in a globally influential organization. If you possess the expertise and drive to excel in this role, we encourage you to apply now and join a visionary team shaping the future of neurology and beyond.

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Skills

Communication Skills
Regulatory Processes
Health Authority Meetings
EMA
MAA Processes
CTA Processes
Strategic Input
International Regulatory Activities
Neurology
US Regulatory Strategies
Cross-Functional Collaboration
CMC
Labeling Considerations
Stakeholder Engagement
Strategic Planning
Problem Solving

Location

Hertfordshire, England, United Kingdom

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