Philip Milliken Email & Phone Number

Stevenage, England, United Kingdom

Responsibilities include therapy indication expansion clinical plan development, leading translational/mechanistic program and the clinical trial biomarker strategy.

Stevenage, England, United Kingdom

Manager of Clinical Translation in the Clinical Development group. Responsibilities include development of mechanism of action aligned to the company’s portfolio, and defining translational biomarker strategies for incorporation on clinical trials.

Stevenage, United Kingdom

Manager and Project Leader in the Disease Biology group, being responsible for multiple projects working in conjunction with our established academic collaborators, to demonstrate the effects of neuromodulation on defined neural circuits in disease conditions.

Stevenage, United Kingdom

Responsible for early-stage biology projects with established academic collaborators across multiple therapeutic areas, to demonstrate effects of neuromodulation on defined neural circuits in disease conditions.

Cambridge, Uk

- Drug Safety Research & Development Lead on multidisciplinary project teams, coordinating non-clinical safety strategies and activities with other lines (e.g. Regulatory, Pharm Sci, DMPK) to achieve project team objectives.- Develop, implement and oversee the non-clinical safety strategy. - Assess potential safety concerns associated with a target under consideration, coordinating with Disease Area and Therapeutic Area Leads to provide an integrated assessment of safety and proposed… Show more - Drug Safety Research & Development Lead on multidisciplinary project teams, coordinating non-clinical safety strategies and activities with other lines (e.g. Regulatory, Pharm Sci, DMPK) to achieve project team objectives.- Develop, implement and oversee the non-clinical safety strategy. - Assess potential safety concerns associated with a target under consideration, coordinating with Disease Area and Therapeutic Area Leads to provide an integrated assessment of safety and proposed de-risking strategies. Show less

Stockley Park, Uk

- Responsible for safety monitoring and evaluation of multiple mature products to meet global compliance and regulatory requirements, both within the pharma and consumer divisions. - Established cross-functional matrix teams, e.g. Safety, Clinical, Labelling, and Regulatory.- Authored periodic regulatory documents (PBRERs, PSURs, RMPs), and providing Local Operating Companies with relevant license renewal documentation.- Conducted safety evaluations, running routine signal… Show more - Responsible for safety monitoring and evaluation of multiple mature products to meet global compliance and regulatory requirements, both within the pharma and consumer divisions. - Established cross-functional matrix teams, e.g. Safety, Clinical, Labelling, and Regulatory.- Authored periodic regulatory documents (PBRERs, PSURs, RMPs), and providing Local Operating Companies with relevant license renewal documentation.- Conducted safety evaluations, running routine signal detection processes, literature reviews, and Safety database searches.- Conducted causality assessment of safety signals, generating evaluation documents in response to internal or regulatory authority requests.- Produced regulatory documentation for updating prescribing information. Show less

Ware, Uk

- Worked within the cardiovascular safety pharmacology group, running non-clinical regulatory studies, establishing new models, with data interpretation, report writing, and producing guideline recommendations. - Study director for regulatory non-clinical cardiovascular safety studies in accordance with the principles of GLP, and designing investigative studies to address specific liabilities.- Data analysis, information collation, interpretation, and report writing to strict… Show more - Worked within the cardiovascular safety pharmacology group, running non-clinical regulatory studies, establishing new models, with data interpretation, report writing, and producing guideline recommendations. - Study director for regulatory non-clinical cardiovascular safety studies in accordance with the principles of GLP, and designing investigative studies to address specific liabilities.- Data analysis, information collation, interpretation, and report writing to strict deadlines.- Advised project teams and designed follow up strategies.- Led and involved with several collaborative data-sharing initiatives internally and externally, to better understand model translation. Show less

Edinburgh, United Kingdom

Wellcome Trust funded project, based on the development of a novel treatment for Acute Renal Failure

Doctor Of Philosophy (Ph.D.), Physiology And Pharmacology

Investigation of the role of superoxide in hypoxic pulmonary vasoconstriction and the development of pulmonary hypertension

Bachelor’S Degree, Immunology And Pharmacology

Education record