Lead Research Scientist - Pharmacology & Toxicology

Placements24; Kimberley; Hybrid; CAD 120,000 - 180,000; Full time

Benefits offered by this job

Competitive salary package

Health insurance

Retirement savings plan

Generous paid time off

Education and conference funding

Job summary

Unknown Client in Kimberley, Canada, seeks a Lead Research Scientist in Pharmacology and Toxicology to advance drug discovery and development. You will lead preclinical studies, design robust assays, and drive safety evaluations.

This role requires a PhD and 7+ years in pharma/biotech, strong leadership, and ability to collaborate across disciplines; GLP experience and publication record preferred. Based at our modern Kimberley facility with competitive compensation.

Qualifications

• PhD in Pharmacology, Toxicology, Pharmaceutical Sciences, or related field.
• 7+ years of pharma/biotech research experience in drug discovery and development.
• Proven expertise in preclinical efficacy testing and toxicology assessment.
• Knowledge of FDA/EMA guidelines.
• Strong scientific writing and presentation skills.

Responsibilities

• Lead in vitro and in vivo studies for drug candidates.
• Develop assay systems for PK/PD evaluation.
• Oversee toxicology studies per regulatory guidelines (GLP).
• Interpret study data and advise development strategies.
• Collaborate with chemists, biologists and regulatory affairs.
• Mentor junior scientists and research staff.
• Prepare study reports, regulatory submissions, and publications.
• Stay updated on pharmacology and toxicology advances.
• Manage project timelines, budgets, and resources.

Skills

Leadership experience

Preclinical pharmacology

Regulatory knowledge

Bioanalytical PK/PD methods

Scientific communication

Education

PhD in Pharmacology, Toxicology, Pharmaceutical Sciences, or related field

Job description

About the Role

Our client, a prominent leader in scientific research and development, is seeking a highly accomplished Lead Research Scientist in Pharmacology and Toxicology to join their dynamic team in Kimberley . This critical role will drive the investigation of drug efficacy and safety profiles, contributing significantly to the discovery and development of novel therapeutics. The ideal candidate will possess extensive experience in preclinical pharmacology and toxicology, a strong track record of leading research projects, and a passion for advancing human health. You will work within a collaborative environment in Kimberley , utilizing state-of-the-art facilities.

Key Responsibilities

• Lead the design and execution of in vitro and in vivo studies to evaluate the pharmacological activity and toxicological profiles of new drug candidates.
• Develop and validate robust assay systems for assessing drug efficacy, pharmacokinetics (PK), and pharmacodynamics (PD).
• Oversee and conduct comprehensive toxicology studies in accordance with regulatory guidelines (e.g., GLP).
• Interpret complex study data, identify potential risks, and make data-driven recommendations for drug development strategies.
• Collaborate closely with medicinal chemists, biologists, and regulatory affairs specialists to ensure seamless progression of drug candidates.
• Mentor and supervise junior scientists and research associates, fostering scientific rigor and professional development.
• Prepare high-quality study reports, regulatory submission documents, and scientific publications.
• Stay current with the latest advancements in pharmacology, toxicology, and drug development methodologies.
• Manage project timelines, budgets, and resources effectively.

Requirements

• Ph.D. in Pharmacology, Toxicology, Pharmaceutical Sciences, or a related discipline.
• A minimum of 7 years of relevant research experience in the pharmaceutical or biotechnology industry, with a focus on drug discovery and development.
• Proven expertise in preclinical drug efficacy testing and comprehensive toxicology assessment.
• Strong understanding of regulatory requirements for drug development (e.g., FDA, EMA guidelines).
• Experience with bioanalytical methods for PK/PD analysis is highly desirable.
• Excellent scientific writing and presentation skills.
• Demonstrated ability to lead research teams and manage complex projects.
• Strong analytical and problem-solving capabilities.
• Ability to work independently and collaboratively in a fast-paced research environment.

Benefits

• Our client offers a highly competitive salary package and a comprehensive benefits program, designed to support the well-being and professional growth of its employees.
• This includes excellent health insurance, retirement savings plans, and generous paid time off.
• Opportunities for continuous learning and development, such as attending international conferences and specialized training, are provided.
• This role is based in our modern research facility in Kimberley , offering a stimulating and collaborative work environment.
• Join a leading organization dedicated to groundbreaking scientific advancements.