医師／九州の求人・転職情報

■Responsibilities: Project Related Medical/Safety Management:

◇Minimize potential risk to PPD and clients by managing medical aspects of contracted tasks. This includes, but is not limited to, medical monitoring of all safety variables (AE, laboratory abnormalities, changes in patient medical status as well as inclusion/exclusion criteria, evaluation prescribed concomitant medication for protocol restrictions and unblinding requests). Scope of work also includes discussion internally with medical monitors in Japan, APAC and global and project team colleagues internally, as well as with principal investigators and clients of all medical issues during the course of a study by proper medical judgment, interpretation and decision.

◇Medical review of serious adverse events: Ensure tasks delegated to medical monitors are properly executed. Adhere to applicable regulations and ICH guidance regarding clinical trials, regulatory documents, and safety issues. Adhere to client SOPs/directives and project specific WPDs for assigned projects. Adhere to PPD’s corporate policies and SOPs/WPDs.

◇Present PPD standard medical processes to clients at business development meetings, investigator meetings, and communicate with various medical communities to explore and expand PPD business.

◇Provide medical consultation to team members and help manage protocol related medical questions. Communicate clearly with project team members and clients, maintaining open communication to ensure all procedures are followed appropriately. Provide therapeutic training and protocol training on assigned studies, as requested.

◇Perform listing reviews as specified in the client contract and data validation manual, including review of coding listings and/or full safety listings as well as use of Patient Profiles and other tools to assess for potential safety signal. This position will be assigned to APAC components of global or regional studies. Including but not limited to global/regional studies with Japan component.

◇This person will also take care of a major responsibility of ICCC review, therapeutic area training to clinical team in PPD-SNBL, supporting business development in PPD-SNBL, and clients requests including F2F visits to investigators, KOLs and sites in Japan.

■診療業務
自由診療における問診・処方判断。
医療カウンセラーが患者様の申込サポートを担当するため、医師は診療に集中いただける環境です。

対応件数目安：診療内容や患者様の状況により変動しますが、多い時間帯で5〜8件/時程度を想定。
既存患者様を引き継ぐ形でのスタートとなるため、ゼロからの集患は必要ありません。
※既存患者様の診療情報の引き継ぎにあたっては、個人情報保護法に基づき、本人同意の取得または適法な第三者提供の根拠を確認したうえで実施します。

■事業推進業務
診療プロトコルの整備・品質管理
診療データをもとにしたサービス改善提案
新診療科目・新メニューの立ち上げ参画
通販・D2Cモデルと連携した医師目線でのフィードバック
広告運用・CS・カウンセラー管理・システム・集客・事務オペレーションはグループ側で体制構築を進めます。
医療機関としての診療品質・安全管理・診療プロトコルの整備については院長として関与いただきますが、それ以外の経営実務は丸投げにはなりません。