■ 職務内容 / Job Description

Responsible for the authoring of clinical-regulatory documents and submission packages that communicate the evidence base of product knowledge in a credible, consistent and compliant way.

■ 応募資格（経験、資格等）/ Qualification (Experience & Skill etc)

【経験 / Experience】

＜必須 / Mandatory＞

• Experience in medical communications gained through working in the pharmaceuticals industry or a medical communications agency
• A comprehensive knowledge of the drug development processes including key regulations/guidelines (e.g. GCP, ICH GLs), and knowledge on a “need to know basis” in relevant therapeutic area.
• Knowledge of policy, standard, SOPs particularly CSP/IC, CSR, IB, CTD

【能力 / Skill-set】

＜必須 / Mandatory＞

• Medical writing skill
• Logical thinking/Presentation skill to express intention in an efficient way in Japanese & English
• Interpersonal and communication skills with team member or stakeholders
• Facilitation skill to lead an innovative solution in conflicting discussion
• Demonstrates aligned behaviours to AZ leadership guideline

【キャリアレベル / Career Level】

D or E level

【勤務地 / Work Location】

Osaka or Tokyo

Date Posted

Closing Date

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.