Location: China-Shanghai-Remote
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 Accountabilities

Derivation of Pharmacokinetic (PK), and Pharmacodynamic (PD) parameters.
Programming and validation of NONMEM datasets and PK/PD derived datasets.
Programming and validation of tables, listings, figures, and statistical appendices if applicable.
Execute activities according to the agreed processes (SOP’s) and timelines while maintaining good quality.
Ensures that the deliveries match the agreed specifications and expectations.
Apply good programming practices; works according to International Conference on Harmonization and Good Clinical Practice standards.
Provides training and guidance and act as a mentor to less experienced analysts.
Checks own work and the work of others to ensure first-time quality.
Maintain a positive, results orientated work environment, building partnerships, and promoting teamwork
Proactively participate in and/or lead process/quality improvement initiatives.
Represent CPMS on cross-functional initiatives
Lead knowledge sharing forums and proactively support the development of the wider department.
May serve as process/system owner responsible for development, implementation and maintenance of process/systems in collaboration with key stakeholder functions (e.g. IT Technology, Quality)

Skills

Expert programming skills (with a focus on SAS or R programming).
Advanced skills in Microsoft applications (Word, Excel, PowerPoint, Outlook)
Unix and/or Linux knowledge is advantageous.
Ability to learn new systems and function in an evolving technical environment.
Professional attitude, self-motivated, logical thinking.
Excellent attention to detail.
Excellent interpersonal, verbal, and written communication skills.
Strong project management skills
Client focused approach to work ethic.
Ability to manage multiple and varied tasks with enthusiasm and independently prioritize workload, demonstrated flexibility to change.
Good standard of written and spoken English
Ability to negotiate and influence to achiever results.
Ability to resolve complex issues in creative and effective ways.
Ability to work well under pressure and to keep to scheduled timelines.
Ability to work with line- and middle-management on a functional level.

4-6 years relevant experience

Expert knowledge of SAS (SAS/BASE, SAS/STAT, and SAS/GRAPH) or R or both

Knowledge of pharmacokinetic data

Understand regulatory requirements concerning industry technical standards

A bachelor’s degree or equivalent in a programming, statistics or mathematics discipline is preferable. Post graduate qualification is advantageous

Additional Locations: China-Beijing-Remote, China-Shenyang-Remote, Taiwan-Remote, China-Guangzhou-Remote, China-Chengdu-Remote

Job description provided by Parexel.
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