A very exciting Senior Regulatory Affairs Specialist (Long term contract, one year continuous renewable as long as you excel and business needs are met) role for a large global leading Pharmaceutical company.
Your new role
Among others, you will be supporting an Associate RA Director handling therapeutic areas such as HCV, Neuroscience, Anesthesia and Specialty Care. You will define and implement regulatory strategies for assigned projects for countries in the JAPAC region in conjunction with various internal stakeholders and represent the JAPAC regulatory function at sub-teams or client group meetings to present regulatory requirements or provide strategic input for the registration of products. You will also have to assesses scientific data provided by specialist units for registration purposes against the different JAPAC national and regional regulatory/clinical requirements, identify gaps and develop mitigation strategies to address these gaps.
What you’ll need to succeed
You will have at least a Pharmacy degree, Biology or pharmacology related subject, at least 5 years’ experience in RA with 3 years’ experience in JAPAC regulatory specialising in new drug applications for NCEs, clinical drug development and clinical trial applications. You must also have in-depth knowledge of the regulatory requirements of the countries within the JAPAC region. Ideally you will be immediately available and must already have the current right to work in Singapore.
What you’ll get in return
A very competitive salary package plus very exciting Senior Regulatory Affairs Specialist (Contract) role with a large global leading Pharmaceutical company.
What you need to do now
If you’re interested in this role, please email me an up-to-date word document copy of your CV, or call me now (email@example.com, 6589 589). If this job isn’t quite right for you but you are looking for a new position, please contact me for a confidential discussion on your career.
A large global leading Pharmaceutical company.