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Job Description & How to Apply Below
This full-time remote role emphasizes scientific leadership in clinical pharmacology, supporting regulatory strategies and compound development plans. With at least eight years in PK/PD and superior communication skills, you’ll mentor teams and stay ahead of industry regulations. Your contributions are vital in crafting documents for regulatory submissions and ensuring quality deliverables.
Key Responsibilities:
• Provide strategic consultation on study design and drug development
• Conduct advanced modeling and data analysis for clinical trials
• Author clinical pharmacology and regulatory documentation
• Support business development and client interactions
• Mentor junior scientists and guide training initiatives
Requirements:
• PhD in Clinical, Medical, or Life Sciences or relevant Master’s
• Minimum 8 years of PK/PD experience in clinical trials
• Proficient in pharmacometrics software like Win Nonlin and R
• Strong communication skills with expertise in medical writing
• Detail-oriented with exceptional organizational abilities
Utilize your pharmacokinetic expertise to elevate drug development processes remotely with Everest Clinical Research.
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