Salary
💰 $202,000 - $336,600 per year
About the role
- Manages and is accountable for the PK/PD evaluation of a small portfolio of products or projects.
- Works independently, with guidance in only the most complex situations.
- Informs PMx management of important program and regulatory developments in a timely manner.
- Ensures analyses and documentation are of the highest quality and accuracy.
- Ensures that reports and other documents have the appropriate messaging and that a meaningful \"story-line\" is developed.
- Ensures that study reports and other documents have an appropriate functional review and are suitable for review by senior management.
- Solves complex problems; takes a broad perspective to identify solutions.
- Has a strong publication record and actively publishes work in scientific literature
- Makes contributions to multi-disciplinary meetings by sharing cross-functional skills and knowledge.
- Has excellent interpersonal and communication skills, both written and oral, and has ability to communicate complex information succinctly.
Requirements
- PhD +8 years with a degree in Quantitative Pharmacology (pharmacometrics) or related field.
- Hands-on usage of a broad range of quantitative tools and systems is required.
- Strong publication record in the field.
- Proven interpersonal and communication skills, both written and oral.
- Proven experience developing QP elements of regulatory strategy and interacting with regulatory agencies without supervision.