Clinical Pharmacologist / Clinical Pharmacologistess

The Life Science Career Network

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

About Our Client

Our client, headquartered in Switzerland—a biotech hub of Europe—is a high-potential biopharmaceutical company specializing in the discovery, development, and commercialization of innovative small molecules. They aim to transform the horizon of therapeutic options and are currently seeking a Clinical Pharmacologist for an initial 24-month contract based in the Basel area.

Position Overview

The Clinical Pharmacologist will contribute to the design, conduct, analysis, interpretation, and reporting of clinical pharmacology trials across drug development. This role provides scientific and medical input to trial teams, supports protocol and trial document development, and contributes to regulatory and cross-functional activities. The position also involves supporting PK/PD data interpretation, trial planning, and the communication of trial results, all while working closely with internal stakeholders under appropriate line management supervision.

Main Responsibilities

• Develop the ability to work independently and flexibly under supervision, delivering high-quality results in a timely manner.
• Proactively gather relevant clinical pharmacology knowledge related to assigned compounds and pursue relevant internal/external training courses.
• Ensure compliance with internal working practices/SOPs, quality control procedures, and regulatory guidelines.
• Lead phase I/IIa studies, including the writing and/or reviewing of clinical trial protocols and other trial-related documents to deliver on time, within budget, and to the required quality standards.
• Contribute to the writing of clinical sections in regulatory or safety-related documents (e.g., Investigator's Brochure, IMPD, briefing books, DSUR, CP sections of NDA).
• Demonstrate a comprehensive understanding of the science related to trial and/or project.
• Respond to scientific/medical inquiries from IEC/IRB and/or Health Authorities.
• Review data prior to database lock.
• Handle all aspects of trial protocols, reports, statistical analysis plans, project summaries, and development plans.
• Prepare or contribute to scientific publications and position papers, including supportive literature reviews.
• Provide input/expertise to the PK/PD section of protocols for phase IIb-IV studies.
• Develop the Clinical Development Plan for the assigned compound in early-stage development (i.e., phase I and II) and/or contribute to it in later stages.
• Elaborate on CP trial plans for assigned projects.
• Maintain contacts with key opinion leaders and investigators.
• Develop line management experience with support from the line manager as necessary.

Shared Responsibilities

• Attend CP group and educational meetings with active contributions (e.g., presentations when requested).
• Contribute to the selection and negotiation with CROs (e.g., clinical, data management, biostatistics, and bioanalytical CROs) and manage monitoring aspects.
• Act as the primary liaison within the CP trial team, providing appropriate input related to medical/scientific aspects.
• Assist in preparing submission documents to Independent Ethics Committees/Institutional Review Boards (IEC/IRB) and Health Authorities.
• Interpret and present trial results to the Life Cycle Team, Development Team, and external audiences as appropriate.
• Collaborate closely with the Modeling and Simulation group within CP.
• Attend scientific meetings and review literature to stay informed about the latest clinical and scientific developments related to the project.
• Represent CP in due diligences and at Health Authority meetings.
• Promote communication and alignment across line functions within the project team.

Qualifications and Experience

• Relevant Swiss working/residency permit and/or Swiss/EU citizenship required.
• Strong academic background, i.e., MSc (or equivalent), preferably a PhD, PharmD, and/or MD.
• 1-2 years of clinical research experience in an academic or industry environment, ideally with drug development experience in a pharmaceutical/biotechnology company.
• Experience in designing, conducting, and analyzing clinical pharmacology studies, including the ability to develop high-quality trial protocols.
• Familiarity with PK/PD evaluation techniques and associated regulatory guidelines.
• Understanding of the roles and responsibilities of relevant functions involved in clinical trials.
• Knowledge of ICH-GCP and other relevant guidance documents/regulations for clinical trial authorization.
• Proficient in interacting with departments involved in drug development.
• Scientific and pragmatic approach to data analysis and interpretation, with attention to detail.
• Highly self-motivated with a proactive working attitude.
• Well-developed interpersonal skills with the ability to act as a team player.
• Clear communication style (verbal and written).
• General IT skills (e.g., MS Office) with the ability to maintain organized documentation and files.
• Willingness and ability to travel as required.
• Capability to carry out PK, PD, and PK/PD analysis using WinNonlin or similar software, and summarize resulting data.
• Adept at working in a matrix environment, managing interactions with multiple stakeholders and providing timely, quality feedback.
• Ability to handle and prioritize multiple tasks in a fast-paced environment.
• Fluency in English is mandatory.

If you would like to learn more about CTC and the opportunity outlined, please apply online using the form below. Only applications matching the job profile will be considered.