Advance groundbreaking drug development strategies in a collaborative environment. Utilize your expertise in PKPD modeling and clinical pharmacology. Contribute to impactful therapeutic innovations and patient care advancements.
Senior Clinical Pharmacology Scientist
in Healthcare + Life Sciences PermanentJob Detail
Job Description
Overview
- Lead clinical pharmacology initiatives to optimize drug development and therapeutic strategies.
- Apply expertise in pharmacokinetics and pharmacodynamics to enhance clinical trial outcomes.
- Collaborate with multidisciplinary teams to ensure successful project execution and regulatory compliance.
- Contribute to protocol design, study execution, and data analysis for clinical trials.
- Utilize advanced modeling and simulation techniques to inform drug development decisions.
- Stay updated on advancements in clinical pharmacology to drive innovation and efficacy.
- Provide critical insights to enhance therapeutic strategies and patient outcomes.
Key Responsibilities & Duties
- Represent Clinical Pharmacology in cross-functional teams, offering expert guidance on PKPD strategies.
- Lead analysis, interpretation, and reporting of pharmacokinetic and pharmacodynamic data.
- Conduct PKPD modeling and simulations to support drug development decisions.
- Prepare regulatory submissions, ensuring compliance and precision in documentation.
- Collaborate with research, bioanalytical, clinical, regulatory, and statistical teams to achieve project goals.
- Design and execute clinical studies, ensuring robust data collection and analysis.
- Stay abreast of literature and advancements in clinical pharmacology methodologies.
- Utilize pharmacometric software to enhance project outcomes and therapeutic strategies.
Job Requirements
- Ph.D. in Pharmacokinetics, Pharmacology, Pharmaceutics, or related field required.
- Minimum 2 years of industry experience, with 3 years preferred.
- Strong knowledge of PKPD principles, modeling, simulation, and clinical pharmacology.
- Proficiency in pharmacometric software such as R, Phoenix WinNonlin, and NONMEM.
- Excellent verbal and written communication skills for collaboration and documentation.
- Ability to work effectively in a matrixed team environment with strong interpersonal skills.
- Experience in regulatory documentation and protocol development for clinical trials.
- Commitment to continuous learning and staying updated on clinical pharmacology advancements.
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