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Senior Principal Scientist: ADME

In a newly formed role, the successful candidate will lead the translation of DM-PK/PD and biopharmaceutics understanding into meaningful product and clinical study design within Seda. Patient centric product development is a key aspect of Seda’s offering, which we believe differentiates us from other organisations, and needs to be built on a sound base of DMPK-PD and biopharm understanding. This is an opportunity to shape the future scientific and strategic direction of the organisation.

Reports to: Company Director

Experience: PhD plus 10 years / BSc plus 15 years

Salary: Competitive plus benefits

Posted: 19th Feb 2021

Closes: 05/03/2021

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In a newly formed role, the successful candidate will lead the translation of DM-PK/PD and biopharmaceutics understanding into meaningful product and clinical study design within Seda.  Patient centric product development is a key aspect of Seda’s offering, which we believe differentiates us from other organisations, and needs to be built on a sound base of DMPK-PD and biopharm understanding. This role will further support our Clients by:

  • ensuring design and selection of candidate drugs with combined DMPK and biopharm properties necessary for development
  • championing biopharm and DMPK-PD integration into product design thinking within Seda and on individual projects
  • Ensuring drugs progress through development with the necessary level of DMPK understanding
  • Ensuring that clinical studies deliver the clinical pharmacology data necessary to support the next phases of development while controlling risk to subjects

Experience:

  • Educated to PhD and greater than 10 years’ translational experience across DMPK, Biopharmaceutics and/or Clinical Pharmacology Sciences or Bachelors degree and greater than 15 years’ translational experience across DMPK, Biopharmaceutics and/or Clinical Pharmacology Sciences

Role Purpose:

  • Seda Pharmaceutical Development Services provide Integrated Pharmaceutical Development and Clinical Pharmacology services and consultancy to the Pharma and Biotechnology Industry
  • The primary purpose of this multidisciplinary role is to provide DMPK, Biopharm and/or Clinical Pharmacology technical leadership to the delivery of Clients’ discovery / development programmes. In addition, there is the opportunity to drive the growth and future direction of the group through interaction with potential Clients and supporting business development activities
  • In your role as Senior Principal Scientist, you will work as part of the Seda team, working closely with colleagues and Clients with an expectation that you will help set the strategic direction of the PK and Modelling function

Role Responsibilities:

The key responsibilities of the role are to:

  • Bring the highest level of scientific thinking together with pragmatic design thinking to deliver candidate drugs and/or development plans, documentation, data interpretation and decisions for Clients’ compounds and products
  • Create value for Clients through strategic and scientific input
  • Act as DMPK / Clinical Pharmacology project leader for Clients’ projects
  • Manage and review CRO activities on behalf of clients
  • Support all aspects of projects as required (across the whole portfolio)
  • Management of the financial aspects of projects with clients, such as costing proposals and invoicing
  • Act as the primary contact for Clients including those based in UK, Europe and USA
  • Author SOPs and / or best practices documents to set the standards for more junior members of staff
  • Act as a mentor to develop the scientific and leadership capabilities of the Seda team
  • Represent Seda at national and international meetings / conferences to build the reputation and awareness of the company
  • Play an active role in the scientific community in your area of expertise
  • Develop business development material such as white papers and technical communications for online posting and attend trade/partnering events
  • Build relationships and manage expectations with Clients
  • Other ad-hoc activities might also be required

 

Person Specification:

  • A publication and candidate drug / drug product delivery record that clearly demonstrates thought leadership in aspects of drug development
  • Evidence of team capability development
  • Experience of drug development and evidence of ability to develop drug products that meet clinical and regulatory requirements
  • Evidence of ability to meet deadlines and targets
  • Evidence of ability to influence and project leadership skills
  • Industrious
  • Self-motivated, able to operate independently and willing to learn and to develop others

 

Location:

  • The role will be based in Macclesfield, Cheshire, UK.
  • Additional travel will be required to attend client meetings, CRO visits and business development events across the UK and abroad. Occasional overnight business travel will be required.

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