Morgan Hunt are currently working with a Professional Regulatory Body in their search for an interim Senior Regulatory Lawyer to provide legal support, advice and leadership to the authorisations team.
You will be responsible for providing legal advice, support and guidance to a team of decision-makers, through utilisation of a complex legal framework and ensuring decisions made are compliant with relevant regulations and guidance.
You will focus on identifying and driving forward change and improvement relating to decision-making and ways of working.
Global Regulatory Affairs - Due Diligence Manager / Senior Manager
This US Biotech are looking for a Regulatory Affairs professional with strong Due Diligence experience to join an exciting, high-profile project, this is initially a 6 month contract but has scope for extension.
The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials.
They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes.
General
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote.
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We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees.
At Mundipharma, we are proud of the work we do to bring innovative treatments to patients.
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SRG are currently looking for a Regulatory Affairs Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead.
The Role
Deliver CTA regulatory strategies and operations for a designated portfolio of development compounds in specified geographic region.
Ensure the submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team and study teams.