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The new drug development manager will work closely with R&D scientists, business executives, suppliers, partner CROs and CDMO/CMC, and other parties to lead new drug development.
The candidate will be involved in the whole process from the early stage of drug development to clinical proof-of-concept (PoC), including the screening and optimization of lead compounds/Antibodies, the determination of preclinical candidate compounds, regulatory filings, and completion of first-in-human trials
The candidate with knowledge with registration and filings procedures with the FDA and NMPA and other key regulatory agencies, as well as various funding organizations will be a plus
The candidate will also be responsible to manage annual planning and budgeting for drug development.
Knowledge related fields include pharmacology, pharmacokinetics, chemistry and manufacturing control, non-clinical safety evaluation, and more.
Requirements
Must be PhD or Post Doc in biology/pharmacology or drug discovery relevant scientific discipline
With 5-10 years’ industrial experience in drug discovery, which may include academic experience at drug discovery institutions
Demonstrated track record in new drug development and research field
Has a strong grasp over budgeting and project planning and control
Abilities
Ability for critical thinking, problem solving and innovation.
Strong organizational and project management skills
Clear and concise communication skills, both oral and written; good interpersonal skills, ability to multi-task, a strong desire to learn, contribute and collaborate
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