Associate Consultant(PRO)

2ヶ月前

Minato IQVIA
【ポジション名】

HEOR Associate Consultant(PRO)

会社紹介・ビジョン

私たちIQVIAは、ヒューマンデータサイエンスの先駆的な企業として、医療・ヘルスケアの前進に取り組む皆様をIQVIAならではの革新的なソリューションによってご支援することで、「誰もが、より健康に自分らしく生きられる社会」の実現を目指しています。世界最大規模を誇る医療・ヘルスケア関連データを基盤に、人・データ・サイエンスを融合させた見地から、未だ満たされない治療ニーズに応える、新たな医薬品や医療機器の開発と市販化、厳格化する規制やコンプライアンスへの対応、持続可能な医療システム推進の支援など、患者さんをはじめとするすべての人々のために、より良い未来へと医療・ヘルスケアを前進させていく力となることが、私たちの使命です。

世界100以上の国と地域で約9万人が活動するIQVIAの日本法人として、IQVIAジャパンでは約6,000人が一丸となり、この使命に向かって日々、力を尽くしています。

【部門について】

HEOR (Health Economic Outcome Research)

IQVIAのコアアセットである医療ビッグデータ、及びテクノロジーを駆使した革新的新薬の市販後観察研究、PMS、Health Economics & Outcome Research(HEOR)研究などのエビデンスジェネレーションを推進

業務内容

Outcome Researchを通じたエビデンス創生(医療・公衆衛生領域)
調査設計(PRO、PCS、DCE、デルファイパネル、実装科学など多様な手法)
インタビュー調査(Concept Elicitation、Cognitive Debriefingなど)
定量・定性解析(テーマ分析、NVivo・Atlasなどのソフト使用)
倫理審査対応(IRB申請、関連文書作成)
研究コンセプト相談から学会発表・論文投稿までのサポート
クライアント向け提案書・報告書作成(日英)
医師・患者・施設スタッフ・患者会との調整・コミュニケーション

条件

公衆衛生・疫学領域での研究経験(医療・製薬関連歓迎)
日本語ネイティブレベル、英語ビジネスレベル(文書作成・会議対応)
タイトなスケジュールや納品対応に前向きに取り組めるストレス耐性

歓迎条件

調査票設計・インタビュー経験
PRO、DCE、デルファイパネル、実装科学の経験
基本的な解析知識(定量+定性)
定性解析スキル(NVivo、Atlasなどのソフト使用経験、テーマ分析)
医師・患者・施設スタッフ・患者会とのコミュニケーション経験
国際共同研究やPublication経験
GCP知識(必須ではないがあれば尚可)

Responsibilities

Conduct Outcome Research to generate evidence in healthcare and public health domains.
Design and implement diverse research methodologies (e.g., PRO, PCS, DCE, Delphi panels, implementation science).
Perform Concept Elicitation interviews (primary focus) and Cognitive Debriefing as needed.
Execute both quantitative and qualitative analyses, including thematic analysis using NVivo or Atlas.
Manage IRB submissions and ethics review processes.

Support the entire research lifecycle:
from concept development to dissemination (conference presentations and manuscript submissions).
Prepare proposals and study reports in Japanese and English.
Communicate effectively with physicians, patients, site staff, and patient advocacy groups.

Required Qualifications

Research experience in Public Health and Epidemiology (preferably in healthcare or pharmaceutical settings).
Hands-on experience in survey design and Concept Elicitation interviews.
Native-level Japanese and business-level English proficiency (document preparation and meeting participation).
Ability to work under tight timelines and deliver high-quality outputs with a positive attitude.
Basic knowledge of quantitative and qualitative analysis.

Preferred Qualifications

Experience with PRO, DCE, Delphi panels, and implementation science.
Strong qualitative analysis skills (NVivo, Atlas, thematic analysis).
Prior experience communicating with physicians, patients, site staff, and patient organizations.
Experience in international collaborative research and publications.
Knowledge of GCP (not mandatory but preferred).

【勤務地】

東京 品川オフィス

【雇用形態・勤務時間・福利厚生・休日休暇】


雇用形態:
正社員

勤務時間:9:00-17:00


フレックス勤務:
あり


在宅勤務制度:
あり 福利厚生:法定内(社会保険制度)・法定外(IQVIA独自制度)の両面から充実した福利厚生制度あり


受動喫煙対策:
あり


休日休暇:
年次有給休暇、夏季休暇、病気休暇、特別休暇、女性特別休暇、育児介護休暇、看護休暇


  • など

試用期間:
あり(通常6か月)

【給与・待遇】


給与:
当社規定により優遇します


昇給:
あり


賞与:
あり


時間外手当:
あり

【選考プロセス】

書類選考~3次面接


IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at
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