Clinical Pharmacology Scientist

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View: 135

Update day: 10-04-2024

Location: Basel Basel-Stadt BS

Category: R & D IT - Software

Industry: Staffing Recruiting

Position: Mid-Senior level

Job type: Full-time

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Job content

Achieva are currently recruiting for an experienced Clinical Pharmacology Scientist to work for one of Switzerland’s largest pharmaceutical companies.This is an initial 2 year contract with the possibility of an extension.The ideal candidate has a clinical pharmacology education with a minimum of a Masters. Has previous experience in an industry setting and has strong experience with PK/PD data analysis.Tasks And Responsibilities
  • Responsible for scientific aspects of clinical pharmacology, including protocol synopsis, consent form, eCRF and protocol amendments
  • Lead the clinical pharmacology data (pharmacokinetics, pharmacodynamics, safety)
  • Lead the ongoing review of study data (PK, PD)
  • Assist in the preparation of the clinical pharmacology component of the project specific investigators
  • Lead the safety review of clinical pharmacology studies and contribute to serious adverse event SAE
  • Responsible for writing final study reports
  • Prepare IND and NDA documentation, the dossiers for meetings
Must Haves
  • MSc, Pharm D or PhD in pharmaceutical sciences, clinical pharmacology sciences (Post Doc considered). (****)
  • +2 years of experience in industry setting (preferably Pharma) supporting clinical pharmacology studies, NCA data analysis, regulatory filings and medical writing. (****)
  • Clinical research experience, preferably in the pharmaceutical industry, with knowledge of ICH GCP and the drug development process (****)
  • Previous experience / working knowledge of various approaches to PK and PD data analysis: compartmental, curve-fitting, non-compartmental. (****)
  • Experience on software: PhoenixⓇ WinNonlinⓇ (plus Microsoft & Google Suites) (****)
  • Experience of working on, and preferably leading a team matrixed around the scientific and/or clinical study-related tasks.
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Deadline: 25-05-2024

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