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See allKey Responsibilities:
- Lead study concept and protocol design, author clinical pharmacology development plans, and create modeling and simulation plans.
- Conduct PK-PD, Pop PK-PD, and related analyses to support clinical trials and ensure accurate data interpretation.
- Prepare and review comprehensive PK/PD analysis reports and provide mentorship to junior pharmacologists.
Qualifications:
- PhD in pharmaceutical sciences, pharmacology, or related discipline with 3+ years experience, or PharmD with 5+ years, or Master's with 7+ years.
- Robust knowledge of pharmacokinetics, pharmacodynamics, and hands-on expertise with WinNonlin, NLME, R, Monolix, and NONMEM.
- Proven ability to manage multiple projects and work effectively in a client-oriented environment.
About ClinChoice:
- Global full-service CRO with over 28 years of experience and 4,000 professionals across the Americas, Europe, and Asia-Pacific.
- Culture driven by mission to accelerate development of innovative drugs and devices, with continuous training and low turnover.
- Equal opportunity employer committed to diversity and inclusivity across gender, race, beliefs, and ethnicities.
ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. With over 4,000 professionals across more than 20 countries, they maintain a quality-focused, collaborative 'one-team' culture that emphasizes work-life balance and professional development.