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【R&D】Associate Director Clinical Development (ADCD), CVRM TA

Plats Kita-ku, Ōsaka-fu, Japan Jobb-id R-065894 Datum inlagd 11/14/2019

【職務内容 / Job Description

Responsible for leading the project planning and operational delivery of Japan clinical work packages in CVRM TA, Japan R&D. The span of activities is broad covering clinical activities in both early and late drug development, registration/submission and post registration product maintenance phases and will include local and global working. 

The role is to lead and manage defined clinical deliverables across a broad range of activities in Japan. This can include the responsibility to lead complex components of a clinical program such as Life Cycle Management, clinical submission activities, or indication development responsibilities or lead independent work packages or maintenance projects.   Tasks involve project planning and operational delivery of clinical programs, and project management of the scope, schedule and budget. In addition to clinical work in drug projects, the J-ADCD may manage improvement or change projects in other business areas.
The J-ADCD may be aligned to one or more projects depending on size and complexity.
The J-ADCD may also cover Japan Clinical Delivery Manager concurrently to the clinical study which requires J-CDM contribution.

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

◆◆経験 / Experience◆◆

<必須 / Mandatory

  • At least 10 years experience from within the pharmaceutical industry or similar large multinational organization.
  • Extensive knowledge of clinical operations, project management tools and processes
  • Proven experience of clinical development / drug development process in various phases of development and therapy areas
  • Experience from leading clinical projects and deliverables or similar expertise from other areas of drug development (such as pharmaceutical development).

◆◆資格 / License◆◆

<必須 / Mandatory

  • University degree( or equivalent), preferably  in medical or biological science or discipline associated with clinical research

◆◆能力 / Skill-set◆◆

<必須 / Mandatory

  • Proven ability to learn by working in multiple phases, TAs and/or different development situations

◆◆語学 / Languages◆◆

<必須 / Mandatory

  • Fluent in spoken and written English for business
  • Native level Japanese

◆◆勤務地 / Work Location◆◆

  • Osaka or Tokyo

◆◆キャリアレベル / Career Level◆◆

  • E


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 authorisation and employment eligibility verification requirements.

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