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Regulatory Affairs Due Diligence Manager

Hays Specialist Recruitment Limited
Posted 14 days ago, valid for a month
Location

Uxbridge, Buckinghamshire UB8 1DH, England

Salary

£50,000 - £80,000 per annum

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Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • Position: Global Regulatory Affairs - Due Diligence Manager / Senior Manager
  • Salary: Good hourly rate
  • Experience required: Strong Regulatory Affairs experience, from early to late stage development and maintenance, ideally with rare disease experience
  • Year of experience required: Not specified
  • Contract length: Initially a 6 month contract with scope for extension

Global Regulatory Affairs - Due Diligence Manager / Senior ManagerYour new companyThis 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. There is the option to be fully remote.Your new roleAs the Regulatory Affairs Specialist, Due Diligence, you will be the regulatory representative for assigned due diligences, under the direction of the Global Regulatory Strategy Lead (GRSL). As a member of a diligence team, you will be responsible for contributing to the diligence on behalf of regulatory affairs and will be empowered to seek optimal strategies and challenge assumptions to meet in-scope objectives and milestones. You will be responsible for the assessment of information that will lead to a regulatory recommendation. In addition, you may be an assigned regulatory representative for a product/s within a therapeutic area. In this case, you will identify and assess regulatory risks associated with product development and define strategies to mitigate risks in alignment with the global business strategy.You may represent the company to the FDA or EMA as well as to corporate partners.What you'll need to succeedMy client is looking for someone with strong Regulatory Affairs experience, from early to late stage development and maintenance and ideally those with rare disease experience.What you'll get in returnGood hourly rate, fully remote working available, the opportunity to be part of a high-profile special projects teamWhat you need to do nowFor more information on this or any other Regulatory Affairs contract jobs, please apply for this advert.If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion about your career.

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.