Clinical Trial Manager II


JoB No. 481
ポジション名 Clinical Trial Manager II
職種 臨床開発
業務内容 臨床試験管理システム(CTMS)、ケースレポートフォーム(CRF)、薬剤管理、安全性、試験マスターファイル(TMF)、IVRS / IWRS登録、データ視覚化ダッシュボード(利用可能な場合)を監視する範囲を順守し、定期的にレビューします。
勤務地 東京都
応募資格 What we’re looking for
・ Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
・ Demonstrated ability to lead and align teams in the achievement of project milestones, demonstrated capability of working with global team members.
・ Knowledge of basic clinical project financial principles
・ Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
・ Must demonstrate good computer skills and be able to embrace new technologies.
・ Consistently clear and effective communication, presentation and interpersonal skills, among project team, sites, and sponor.
・ Ability to apply problem solving techniques to resolve complex issues, and apply a risk management approach to identifying and mitigating potential threats to the successful conduct of a clinical research project.
・ Demonstrates adaptability to change; new processes, systems, etc.
・ Demonstrates critical thinking to determine the cause and appropriate solution in the identification of issues
・ Moderate travel may be required, approximately 20%
Additional Information:
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

雇用形態 正社員
年収目安 800万〜1200万円
担当コンサルタント 吉原 貴