Clinical Pharmacologist (6687 – KFR)

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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 have a long-standing relationship with this company and have placed a number of key people in the organisation in the past, all of whom have given us some great feedback from their time working there.

We are currently looking for a Clinical Pharmacologist for a
9- to 12-month contract (maternity cover) 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
• Knonwledge in Antiinfectives is desirable
• English fluent
• Experience with MS Office, Phoenix, WinNonlin
• Team working ability, flexible and open personality