You will be responsible for overall safety information management tasks. This includes primary evaluation of clinical trials, post-marketing safety information, and literature society assessments within Japan. You will support the monitoring of domestic cases, provide instructions for further investigation to medical representatives, and conduct primary evaluations and translations of overseas safety information in English, including CIOMS and Med Watch forms. Responsibilities also involve creating reports for adverse effects and other incidents to the PMDA, including SGML formatting. The company provides management support for compound, reagent, and solution management, CMC, trial planning, protocol creation, case registration, drug allocation, progress management, CRA/DM, analysis, safety information response, and audit operations. EPS is the largest domestic CRO in Japan, has a strong company culture that prioritizes employee welfare, and maintains a low turnover rate despite a high number of mid-career hires.
The above information is a public job ad. This job ad is neither an offer nor a contract.
Join Now
Free โข No credit card โข Done in seconds
Apply with this intro
Using an intro message in your application increases your % of getting hired.
Apply with this intro
Ok
Save
Save
Save
Apply for this position
I have a favour to ask. When you apply to EPS Corporation, please tell them that you heard about the position on EPIC JAPAN. This helps to keep this job board sustainable, so I'd be greatful for your support with this.
โ Kevin, Founder of EPIC JAPAN
Continue applying
๐ฅ Most Popular Jobs in Japan ๐ฅ
Jobs in Japan by Languages
Jobs in Japan by Location
Jobs in Japan by amenities
By specific Japanese levels
Other Jobs in Japan
Add your CV so we can match you with jobs in Japan.
Save
No more endless applications.
Continue with Google
So that companies can contact you