Clinical Pharmacologist - Phase I Trials Lead (12-24m)

CTC Resourcing Solutions AG; Basel; On-site; CHF 120,000 - 180,000; Full time

Job summary

CTC Resourcing Solutions AG is assisting a Swiss-based biotech company in Basel seeking a Clinical Pharmacologist for a 24-month contract. The role involves design, conduct, analysis, and reporting of clinical pharmacology trials, with close collaboration across trial teams and regulatory activities.

Responsibilities include leading CP studies, contributing to regulatory documents, PK/PD interpretation, and trial planning. Fluency in English is mandatory and a Swiss permit is required.

Qualifications

• Swiss working/residency permit and/or Swiss/EU citizenship required.
• Fluency in English is mandatory.
• 2-4 years of hands-on clinical research experience in academic or industry, preferably drug development in pharma/biotech, mainly in phase 1.
• Experience in designing, conducting, and analysing CP studies and in elaborating CP trial protocols.
• PK/PD evaluation techniques and related regulatory guidelines.
• Ability to carry out PK, PD, and PK/PD analyses using WinNonlin or similar software.

Responsibilities

• Lead and conduct CP studies including writing and reviewing trial protocols and related documents.
• Provide input to regulatory or safety-related documents (IB, IMPD, DSUR, CP sections of NDA).
• Support PK/PD data interpretation, trial planning and communication of trial results.
• Collaborate with trial teams and stakeholders with strong line management supervision where applicable.
• Represent CP in project teams and contribute to regulatory submission documents.

Education

MSc (or equivalent)

PhD/PharmD/MD

Tools

WinNonlin

Job description

CTC Resourcing Solutions AG is assisting a Swiss-based biotech company in Basel seeking a Clinical Pharmacologist for a 24-month contract. The role involves design, conduct, analysis, and reporting of clinical pharmacology trials, with close collaboration across trial teams and regulatory activities.

Responsibilities include leading CP studies, contributing to regulatory documents, PK/PD interpretation, and trial planning. Fluency in English is mandatory and a Swiss permit is required.