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RBW are partnered with a global biotech organisation that are seeking an experienced and driven Associate Director in Clinical Pharmacology to support a rapidly growing portfolio of therapeutics targeting central nervous system disorders. This role offers a unique opportunity to contribute to cutting-edge clinical development in a dynamic and collaborative environment. Responsibilities: • Serve as the clinical pharmacology lead providing scientific and strategic guidance to project teams, • Provide guidance for dosing regimen and informing best strategy for modelling techniques, • Perform PK and PK/PD analyses to support clinical trial design and execution, • Contribute to regulatory submissions, including briefing documents, INDs, CTAs, and NDAs, • Overseeing development of junior clinical pharmacology scientists, • PhD in clinical pharmacology, pharmacokinetics or a relevant field, • Extensive experience in the pharmaceutical or biotech industry, with a strong background in clinical pharmacology and PK/PD modeling, • Previous hands on Population PK/PD modelling and simulation experience is desirable, • Strong knowledge of clinical pharmacology guidelines for regulatory submissions, • Proficient user of NONMEM, Phoenix WinNonlin, R etc

As Clinical Trial Manager you will be responsible for providing support or leading specific activities for the planning, set-up and execution of assigned drug trials which may include: pre/post-POC interventional drug trials, Clinical Pharmacology normal healthy volunteer clinical trials, pre-approv

Jazz Pharmaceuticals is an equal opportunity/affirmative action employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.

Strong knowledge of clinical pharmacology guidelines for regulatory submissions. RBW are partnered with a global biotech organisation that are seeking an experienced and driven Associate Director in Clinical Pharmacology to support a rapidly growing portfolio of therapeutics targeting central nervou

Serve as the clinical pharmacology Lead at cross function teams, and responsible for the dose selection and rationale in phase 1 studies and contribute to dose selections in clinical studies beyond phase 1. Identify and manage consultants and vendors supporting clinical pharmacology studies. Contrib

Serve as the clinical pharmacology Lead at cross function teams, and responsible for the dose selection and rationale in phase 1 studies and contribute to dose selections in clinical studies beyond phase 1. Identify and manage consultants and vendors supporting clinical pharmacology studies. Contrib

The Senior Clinical Project Manager (SCPM) is responsible for managing the trial from set-up through to the clinical and post-clinical phases, overseeing the operational delivery of our clinical trials. Richmond Pharmacology are an early phase Clinical Research Organisation (CRO), conducting pioneer

The CPL works cross-functionally with various teams, including but not limited to discovery research & non-clinical functions, clinical science, clinical biomarker, clinical operations, biometrics & data science, and regulatory affairs, to ensure the clinical pharmacology aspects of drug development

Extensive experience in the pharmaceutical or biotech industry, with a strong background in clinical pharmacology and PK/PD modeling. Strong knowledge of clinical pharmacology guidelines for regulatory submissions. RBW are partnered with a global biotech organisation that are seeking an experienced

The SCPM is responsible for managing the trial from set-up through to the clinical and post-clinical phases, overseeing the operational delivery of our clinical trials. Richmond Pharmacology are an early phase Clinical Research Organisation (CRO), where we are conducting pioneering early phase healt