Associate Regulatory Affairs Director

2 weeks ago

Cambridge Cambridgeshire, United Kingdom Gilead Sciences, Inc. Full time

Global Regulatory Affairs, Associate Director (Oncology) page is loaded Global Regulatory Affairs, Associate Director (Oncology)
Bewerben locations United Kingdom - Cambridge United Kingdom - Uxbridge time type Full time posted on Vor 2 Tagen ausgeschrieben job requisition id R0040717 For Current Gilead Employees and Contractors:
For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.we’re nurturing them to foster an environment of inclusion and growth where innovation is encouraged. We expect our people leaders to model that environment, and to focus on creating inclusion, developing talent, and enabling teams.Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact. Join Gilead and help create possible, together.
We are looking for a driven individual who is passionate about bringing transformational medicines to those in Europe and international countries with continued unmet medical need.
This is an exciting opportunity for a Regulatory Affairs Associate Director to join the Gilead Global Regulatory Affairs Oncology team to support drug development and registration of oncology assets. In this role you will need to provide provide regulatory strategy, leadership, and operational support for Gilead’s growing oncology development product portfolio, allowing you to strengthen your drug development and regulatory expertise . In the role you will be expected to work cross-functionally with a diverse number of stakeholders both internally and externally to Gilead Global Regulatory Affairs.
Defines the regional regulatory strategy for development or marketed products, taking in consideration the latest precedent, regulatory intelligence, agency communications, and guidance.
Represents Gilead in discussions and at meetings with regulatory authorities (as required).
Works closely with Global Regulatory Leads to agree and ensure delivery of the local regulatory strategy to cross-functional leaders and teams.
Acts as representative for specific indications at Regulatory Project Team, and with cross-functional teams, for specified regions and products.
Study Management, Clinical, Nonclinical, Biomarkers) or assign such to other colleagues and oversee and guide their sub-team participation as required.
Responsible for the content, preparation of moderately complex regulatory submissions, and their optimal execution in alignment with business needs.
Ensures regional product labelling is created and maintained in alignment with the Company Core Data Sheets and Company Core Safety Information.
Able to use internal electronic systems for planning, preparing, tracking, and storing submissions to regulatory agencies.
Contributes to the culture of continuous improvement across regulatory affairs helping team members learn and develop aspects of regulatory strategy and research, to lead or contribute to regional strategies.
Teamwork •Excellence •Accountability •Integrity •Inclusion
Detailed understanding of European Medicines Agency (EMA) regulatory requirements and International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) standards for medicinal products. Understands varying regional or country regulatory requirements for assigned markets.
Knowledge of current global and regional trends in biopharmaceutical regulatory affairs. Clear ability to lead cross-functional teams, and develop, communicate, and implement regulatory strategy.
Excellent verbal and written English communication skills, and demonstration of excellent interpersonal skills.
Excellent planning and organisational skills with the ability to work simultaneously on multiple projects with tight timelines.
Life science degree and demonstrated broad and/or depth of experience in pharmaceutical regulatory affairs across at least the European region, including leadership of major applications and health authority interactions.
Three days a week (Tues/Wed/Thurs) at the Stockley Park (Greater London) or Cambridge UK offices.
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual’s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.

For Current Gilead Employees and Contractors:
The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.
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