太陽光発電所・風力発電所・系統用蓄電池の事業開発・建設・維持管理に関して土木領域の技術者として社内外の関係者との協議・調整業務を行う。このポジションに最適な人材は、組織能力に優れ、積極的で、コミュニケーションに長け、さまざまなチームのニーズに適応できる人材です。 · ...

臨床研究サイトおよび臨床試験参加に関する患者データおよび研究関連情報を監視します。調査員が研究プロトコル、規制要件、良好な臨床慣行に従い、データ検証計画への入力を提供します。患者データのタイムリーかつ正確なモニタリングと、ソースドキュメント、研究記録、およびサイト訪問から、必要に応じて調査関連情報を提供します。 · 調査サイトおよび監査施設の選択を監視します。 · 臨床試験を実施する能力を評価するために、潜在的なサイトのサイト選択を実施します。 · さまざまな問題を解決するための会社の方針と手順を適用します。 · コスト センターの目標と目標に貢献します ...

Clinical Site Associate role at ICON plc in Tokyo Osaka with office hybrid setup. ...

Clinical Site Associate - Office Hybrid role at ICON plc in Tokyo Osaka, fostering an inclusive environment driving innovation and excellence. · Competitive salary and benefits package. · Diverse culture that rewards high performance and nurtures talent. · ...

ダビンチサージカルシステムの稼働率を最大化する責務を担い、各地域の市場に合わせたコンサルティング型の営業活動を実施し、新製品の紹介や消耗品等の販売を行う。 · 主要な手術手技におけるダビンチ手術の専門家として、手術チームの「パートナー」としての地位を確立する。 · ...

臨床研究サイトおよび臨床試験参加に関する患者データおよび研究関連情報を監視します。調査員が研究プロトコル、規制要件、良好な臨床慣行に従い、データ検証計画への入力を提供します。患者データのタイムリーかつ正確なモニタリングと、ソースドキュメント、研究記録、およびサイト訪問から、必要に応じて調査関連情報を提供します。 · 臨床試験を実施する能力を評価するために、潜在的なサイトのサイト選択を実施します。 · サイト開始訪問を実行し、サイトのスタッフがすべての試験関連の側面に完全に訓練されていることを確認します · さまざまな問題を解決するための会社の方針と手順を ...

Clinical Site Associate in Tokyo Osaka - Office Hybrid at ICON plc, a world-leading healthcare intelligence and clinical research organization. · ...

Join our international team and be the key support to clinical research projects, streamlining communication, maintaining systems and managing documents & information. · Maintenance of databases and tracking systems · Serves as the primary sites' contact point for vendors, study ...

+Execute bioequivalence studies pharmacodynamic studies clinical endpoint studies healthy subjects patients accordance GCP regulatory requirements assistance Manager Vender Management documents PMDA consultation collaboration local regulatory affairs global team prepare submissio ...

We are currently seeking a full-time Associate Director/Director to join our Site Contracts team in Tokyo. · This role will be responsible for the strategic development of the group, management of the team, and continuous improvement of processes. · As a leader of the Site Contra ...

Deep Intelligent Pharma is pioneering the transformation of the pharmaceutical industry with a revolutionary AI-native, multi-agent platform. Our mission is to empower pharmaceutical and medtech innovators by turning regulatory and clinical complexity into a catalyst for speed, s ...

We are searching for a knowledgeable, team-oriented CRA II to manage the clinical aspects of full-service global projects in Japan. · Conduct and report all types of onsite monitoring visits · Be involved in study startup · Perform CRF review, source document verification and que ...

Civil Site Associate responsible for conducting civil design work, overseeing cost estimation processes, and supervising construction processes. · Conduct civil design work as per project specifications and regulatory requirements. · Oversee cost estimation processes and schedule ...

We are seeking a Associate Clinical Trial Manager to join our Clinical Trial Management team in Tokyo. The ideal candidate will have a PhD in Life Sciences and/or Post-Doctoral Research experience, with excellent analytical and academic skills. They should be able to transfer and ...

We're searching for a knowledgeable, team-oriented CRA II to manage the clinical aspects of full-service global projects in Japan. As a CRA II at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical ...

We are seeking an Associate Director, Clinical Development to play a key role in the scientific planning, execution and reporting of Japanese clinical studies for Gilead's development compounds in inflammation and virology therapeutic area. · ...

Responsible for preparing, negotiating, and finalizing agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. · ...

We are seeking a Senior Clinical Research Associate I to work on the frontline of communication with project stakeholders, ensuring timelines, targets. You will have the opportunity to work on clinical studies in various therapeutic areas and indications while maintaining the hig ...

Responsible for preparing, negotiating, and finalizing agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. · ...

Responsible for preparing, negotiating, and finalizing agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. · Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements ...

Responsible for preparing, negotiating, and finalizing agreements and budgets related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. · Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements ...