◔ Full-Time
➣ Location: Shanghai, China
☉ Junior-Middle Level
Responsibilities
- Support Toxicology and Safety and work with colleagues on outsource study activities to meet the set timeline within the budget with high quality
- Monitor assigned studies including scientific protocol design, data analysis and reporting with supervision
- Manage study related activities including contract, timeline/cost/budget tracking
- Work with business development team activities to win business
- Review scientific report and generate slides deck for project team and client presentation.
- Be able to cross functionally with other stakeholders as well, especially, discovery, CMC, clinical, finance, procurement, office administration, and GLP compliance.
Skills & Requirements
- Bachelor or MSc degree or equivalent in a biological, scientific, or health-related discipline, postgraduate degree (PhD) is preferred.
- 2-5 years’ experience in scientific related role in the pharmaceutical industry or CROs, experience in large molecule drug discovery and development is a plus.
- Experience at CRO is a plus
- Understand the basic principle of GLPs and familiar with ICH, FDA and NMPA guidelines
- Ability to read, communicate in English (written and oral) and collate scientific and research literature.
- Excellent verbal and written communication, excellent interpersonal and information management skills.
- Collaborate effectively with the study team, cross-functional team members, and external partners.
If you are interested in joining our team, please send your resume to our HR department at nona.hr@nonabio.com.
