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Clinical Pharmacologist KFR

Job in 4040, Basel, Kanton Basel-Landschaft, Switzerland
Listing for: CTC Resourcing Solutions
Seasonal/Temporary position
Listed on 2025-11-21
Job specializations:
  • Healthcare
    Clinical Pharmacist
Salary/Wage Range or Industry Benchmark: 30000 - 80000 CHF Yearly CHF 30000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Pharmacologist (6687 – KFR)

2 days ago Be among the first 25 applicants

Direct message the job poster from CTC Resourcing Solutions

CTC is a specialized search and recruitment partner for the Life Sciences industry, serving clients and candidates since 1997. We enable careers by connecting talented professionals with meaningful opportunities, and we support our clients in engaging, retaining, and developing the right talent when needed.

Clinical Pharmacologist

Our client is an innovative mid‑size pharmaceutical company with global headquarters in the German‑speaking part of Switzerland. A well‑funded and stable organisation, our client enjoys the backing of a number of leading, globally recognised institutions. We are currently looking for a Clinical Pharmacologist for a 9‑ to 12‑month contract (maternity cover, with possibility for extension) based in Basel, Switzerland.

Main Responsibilities
  • Support clinical pharmacology studies and lead clinical pharmacology study conduct together with the Clinical Operations Manager
  • Perform clinical PK analysis
  • Support all the functions relevant to the conduct of a clinical study in healthy subjects
  • Write/contribute to clinical study protocol
  • Prepare and review clinical trial documents (Kick‑off meeting slide, site activation, lab manual, pharmacy manual, SAP, IMP labels, drug supply request, Protocol deviations…)
Qualifications and Experience
  • Relevant working/residency permit or Swiss/EU‑Citizenship required
  • PhD in Clinical Pharmacology and/or Pharmacokinetics PK
  • Hands on experience in running and leading Phase I healthy volunteer clinical studies:
    Writing/reviewing study manuals – protocol, clinical study report, dosing, labeling, daily review, and monitoring of the study data
  • Experience in leading Phase 1 trials in healthy subjects for at least 5 years
  • Knowledge of clinical pharmacokinetics, clinical pharmacology study conduct (hands‑on), clinical study documentation preparation, clinical CRO management, patient profile review, clinical PK analysis
  • Knowledge in Antiinfectives is desirable
  • Experience with MS Office, Phoenix, Win Nonlin
  • Team working ability, flexible and open personality
Seniority level

Associate

Employment type

Temporary

Job function

Science and Project Management

Industries:
Pharmaceutical Manufacturing and Biotechnology Research

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