Job offers for Clinical Pharmacology jobs in the United Kingdom

Top Job | Fulltime |

Duties - Entry of relevant/required safety data into the Global Safety Database from spontaneous sources, clinical trials and other solicited sources - Provision of safety information/acknowledgement to marketing partners/other third party partners/Global Medical Safety within the internal and

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Top Job | Fulltime |

Clinical Pharmacology Scientist. If you thrive in a fast-paced, customer-focused scientific environment, working daily with pharmaceutical and clinical data then this role is for you. Reporting to the Chief Scientific Officer and working closely with our commercial and operational teams throughout

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21/04/2018 | Fulltime |

Company Overview Our growing and successful business comprises of over 700 talented individuals globally, in an environment where everybody counts and is instrumental to our success. With state-of-the-art manufacturing and clinical facilities in the UK and USA, we deliver a full range of drug

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Director Pharmacology and Translational Sciences JOB PURPOSE Lead the development of new models to drive the progression of projects within the Immuno Oncology (IO) portfolio Work with the VP of IO to refine the company's IO strategy, improve capacity (by introducing new technologies) and

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Either Formulation Development, Clinical Manufacturing, Phase I and/or Clinical Pharmacology. Preferably of more than one. We are seeking a tenacious professional who can self-build a robust business pipeline by spotting project opportunities from direct interactions with pharma and biotech companies

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19/04/2018 | Fulltime |

Safety data into the Global Safety Database from spontaneous sources, clinical trials and other solicited sources - Provision of safety information/acknowledgement to marketing partners/other third party partners/Global Medical Safety within the internal and contractual timelines - Requesting additional

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19/04/2018 | Fulltime |

Safety data into the Global Safety Database from spontaneous sources, clinical trials and other solicited sources - Provision of safety information/acknowledgement to marketing partners/other third party partners/Global Medical Safety within the internal and contractual timelines - Requesting additional

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17/04/2018 | Fulltime

Balanced clinical and scientific information that supports the appropriate use of our products and services - Identify and communicate key clinical and research issues from KOLs to appropriate departments In order to be considered for this role, you will be required to have the following qualifications

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You will use your clinical pharmaclogy expertise to inform dosing algorithms and a clear strategic plan for clinical development. The role will involve - Acting as a project rep to communicate PK/PD activities. - Delivering Quantitative Clinical Pharmacology strategic planning. - Accountable for non

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Education and information on products Further responsibilities will include - Support product launch activities and communication plans, develop and implement regional strategy and tactical plans - Respond to customer inquiries to ensure focused and balanced clinical and scientific information that

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17/04/2018 | Fulltime |

Database lock, sound knowledge of ICH-GCP and good organisational skills. Lead study and project teams in the delivery of high quality data to support the reporting of early phase clinical pharmacology studies. Close collaboration with investigational sites and monitors around the world in the setup

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17/04/2018 | Fulltime |

Database from spontaneous sources, clinical trials and other solicited sources. -Provision of safety information/acknowledgement to marketing partners/other third party partners/Global Medical Safety within the internal and contractual timelines -Requesting additional information from multiple sources

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Top Job | Fulltime

Relevant, complete accurate and timely compliant, high-standard, and customized scientific answers to medical educational requests by external (Health Care Professionals (HCPs) and by internal customers (employees and consultants) with the supported documentation as Standard Medical Letters, Clinical

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Top Job | Fulltime |

From database set-up to database lock, sound knowledge of ICH-GCP and good organisational skills. Lead study and project teams in the delivery of high quality data to support the reporting of early phase clinical pharmacology studies. Close collaboration with investigational sites and monitors around

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