Offer summary

Qualifications:

M.S., Pharm.D, PhD or equivalent degree in pharmacometrics, pharmacokinetics, clinical pharmacology, statistics, or related discipline., Experience with pharmacostatistical methods of data analysis and study design is essential., Candidates with backgrounds in mathematics, engineering, or systems biology will be considered if they have relevant experience., Excellent verbal and written communication skills in both Chinese and English are required..

Key responsabilities:

Provide pharmacometrics expertise and leadership to projects.

Develop model informed drug development plans to optimize studies and inform drug development strategy.

Conduct and report quantitative analyses integrating pharmacokinetics, pharmacodynamics, and patient characteristics.

Act as a pharmacometric Subject Matter Expert, supporting methodology development and training within the global clinical pharmacology organization.

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

KEY RESPONSIBILITIES:

1. Provides pharmacometrics expertise and leadership to projects.

2. Develops model informed drug development (MIDD) plans across projects and disease areas in order to optimize prospective studies, inform drug development strategy and project decision-making, in collaboration with partners.

3. Conducts and reports quantitative analyses which integrate knowledge of pharmacokinetics, pharmacodynamics, patient characteristics, and disease states to optimize doses, dosage regimens and study designs throughout clinical drug development.

4. Identifies opportunities where modeling and simulation can advance the understanding of pharmacological activity, efficacy and safety.

5. Acts as pharmacometric Subject Matter Expert (SME), including proactive support and development of quantitative methodology, software, hardware, and related business processes, in addition to training to the the global clinical pharmacology organization.

Minimum Requirements

An interest and experience of pharmacostatistical methods of data analysis and study design are essential.

Ideal qualifications include M.S., Pharm.D, PhD or equivalent degree with training and/or expertise in one or more areas related to pharmacostatistical modeling (e.g., pharmacometrics, pharmacokinetics, clinical pharmacology, statistics, or related discipline).

Candidates from alternative backgrounds (e.g. mathematics, engineering, system biology, medicine) will be considered if they can demonstrate relevant experience and expertise.

Communication Skills: demonstrates excellent verbal and written communication skills (both CN and EN)

Required profile