Senior Pharmacometrics Director

2 weeks ago

Melbourne, Victoria, Australia Certara Full time
About Certara

Certara is a leading provider of advanced drug development solutions, dedicated to accelerating the creation of innovative medicines that make a meaningful impact on society. With a dynamic and collaborative work environment, we foster a culture of innovation, creativity, and continuous learning.

The successful candidate will play a pivotal role in driving the growth and strategic direction of our pharmacometrics organization, working closely with senior leadership to develop and implement business strategies that optimize resource allocation and maximize client engagement.

Job Responsibilities
  • Lead complex projects, including hands-on contributions to select initiatives, and serve as a senior resource for project teams reviewing work product and discussing project strategy.
  • Coordinate QSS leadership meetings, drive agenda, monitor follow-up, and optimize meeting cadence and attendees as needed.
  • Develop and implement robust resourcing approaches, ensuring balanced utilization across teams, and partner with Operations to identify under/overutilized resources.
  • Support IDD Operations with process implementation and optimization within QSS, ensuring seamless integration with commercial and operations teams.
  • Recruit and manage talent acquisition, ensuring hiring targets are met while maintaining organizational balance and skills distribution.
  • Lead special projects aimed at strengthening global footprint and effectiveness of QSS consultancy operations.
  • Promote collaboration and knowledge sharing across CDDS and Certara business units, fostering a culture of open communication and mutual support.
Requirements and Qualifications
  • PhD, MD, PharmD in Pharmaceutical Sciences, Pharmacology, Toxicology, Statistics, Mathematics, or related fields.
  • A minimum of 10 years' industry/consulting experience, combining academic research and practical application in R&D, preclinical, and clinical environments.
  • Demonstrated expertise in pharmacometrics, clinical pharmacology, PK/PD modeling, and statistical analysis, with strong understanding of regulatory agency interactions.
  • Experience in moving compounds through development phases, clinical trial design, conduct, and regulatory filings, with excellent writing, editing, and verbal communication skills.
  • Ability to lead company initiatives, mentor others, and drive business development efforts, with a strong track record of delivering results-oriented solutions.
  • Excellent interpersonal skills, ability to build strong relationships with clients, colleagues, and stakeholders, and contribute to a positive work environment.
About This Opportunity

We offer an attractive salary package of $120,000 - $180,000 per annum, commensurate with experience, plus benefits and opportunities for professional growth and development. As an equal-opportunity employer, we welcome applications from diverse candidates who share our commitment to excellence and innovation.

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