You will be tasked with preparing various documents related to new drug deverlopment and applications including CSR (Clinical Study Reports), product summary, Gaiyo summary, and CTD.
- We are looking for individuals who are well-versed in the fields of pharmacology, toxicology and drug design with 3 or more years of experience who in the past 3 years either prepared or pariticipated in document preparation projects of the various document types listed above.
- Individuals with experience in clincial development at pharmaceutical companies, application approval or CRO support are preferred.
Various benefit programs are provided
- Insurance: employment insurance, workers’ accident compensation insurance, medical insurance, employees’ pension insurance
- Retirement allowance: the employee will be entered into a retirement allowance mutual aid
- Other: company-designated resort facility
【Benefits outside Japan】
Benefits including health insurance, employee insurance and pension insurance etc. are decided upon consultation with the company.