Location **Human Factors Drug Delivery Lead**
Location: Raleigh Discipline: Human Factors Salary Details: Competitive + Benefits Advertising End Date: Not Specified *
* Human Factors Drug Delivery Lead
About The Role As Human Factors Drug Delivery Lead your role will be to provide strategic guidance to our pharmaceutical clients and internal HF team on the application of human factors engineering for drug delivery devices and associated products such as regulated mobile companion applications. The leadership you provide will extend to the identification, scoping and implementation of human factors research activities to support the development of early-stage concepts, optimisation of user interfaces and the validation of drug delivery devices and associated products. In this external-facing role, you will be comfortable interacting with clients in a business development context, providing human factors recommendations and working collaboratively with client teams such as clinical, regulatory and product development, as well as providing thought leadership at relevant pharmaceutical industry events. Cambridge Design Partnership is a leading technology and product design consultancy headquartered in Cambridge, UK, managing and delivering global projects for innovative consumer and healthcare companies. Youll work alongside our cross-disciplinary user-centred design team in this unique, dynamic and innovative environment About You
* Good degree in Product Design, Engineering, Human Factors, Psychology or Social Sciences related field
* Experience in scoping and managing human factors programmes for pharmaceutical companies from concept to validation including and being responsible for quality, costs and planning.
* Extensive experience in designing, moderating and reporting on usability studies for drug delivery devices and associated products (both formative and summative including when integrated into clinical trial protocols)
* An in-depth knowledge of human factors regulatory requirements for drug delivery devices within the context of drug development programmes
* Demonstrable experience of translating research into usability engineering documentation in line with FDA & EU requirements
* Extensive experience collaborating with individual from clinical, regulatory affairs and product development within pharmaceutical companies to deliver human factors programmes.
* Excellent presentation, communication and
interpersonal skills which you will apply to build relationships with clients and cross disciplinary development teams, mentor junior staff, and provide thought leadership at global industry events
* Strong drive to rapidly absorb and develop skills and apply these to a wide range of projects
* Experience of the following would be an
advantage; the application of human factors to OTC products, regulatory frameworks for regulated mobile applications, labelling and training design and risk management(Subject to COVID-19 restrictions)
* A willingness to travel for undertaking research or attending global conferences for up to a week at a time
We are an employee owned company with our staff at the centre of our strategy. Employee ownership allows us to maintain full control over the direction of our business and our creative culture. Work Authorization
Cambridge Design Partnership will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided.
Equal Opportunity Employer
Cambridge Design Partnership is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, marital status, political affiliation, sexual orientation, gender identity, genetic information, disability or protected veteran status. We are committed to providing a workplace free of any discrimination or harassment.
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