どんな仕事かAIによる生成

Provides project management and leadership for large-scale and/or complex clinical programs, leading clinical project team members to complete deliverables within agreed timelines. The role oversees clinical trials, manages trial budgets and timelines, and coordinates with internal functions and clinical sites.

応募資格・募集要項・仕事内容を見る

応募資格

必須

Bachelor’s-level degree required. Degree in science/health related field (e.g., Biology, Nursing, Biomedical or Veterinary Sciences) preferred.
8+ years experience in clinical/scientific research, nursing, or medical devices/pharmaceutical clinical trials plus 3+ years experience managing projects and working with clinical professionals within a team, as well as working in a cross-functional product development setting.
Ability to understand strategic goals and match the business needs of the company.
Ability to develop good interpersonal relationships with clinical / medical professionals.
Good verbal and written communication and presentation skills.
Must be familiar with the laws, regulations, standards and guidance governing the conduct of clinical studies.
Ability to independently manage and provide significant tactical and leadership guidance to clinical team.
Independently motivated.
Demonstrated previous success managing multiple, complex, and international projects.

歓迎

Masters-level degree (or equivalent), or qualification in clinical trial management / medicine preferred.
Previous experience with complex, global trials is preferred.

募集要項最終確認 11/4

職種: 臨床開発・薬事
雇用形態: 記載なし
給与: 記載なし
給与の詳細: N/A
勤務地: Hamarikyu Park Side Place 9F, 17F 5-6-10,Tsukiji,Chuo-ku
働き方: 記載なし
経験年数: 8年以上
学歴: 大学卒業以上
掲載日: 2026/10/13 06:25（23日前）
最終確認: 2026/11/04 20:22（1日前）

仕事内容

Primary Function

Provides project management and leadership to plan, prepare and execute high quality large scale and/or complex clinical program(s). Leads the clinical project team members toward completion of deliverables in a timely fashion within an agreed project timeline. Internally interfaces with data management, biostatistics, clinical research associates, business leads, medical directors, functional management, and acts as a company liaison with site investigators and clinical site staff.

Major Responsibilities

Responsible and accountable for several (possible global) clinical trials.
Responsible for ensuring the trial is “audit ready” at all times (project team training records, central files, system validation, etc.).
Leverages resources, expertise, and knowledge across multiple projects to ensure attainment of project deliverables.
Responsible for effective communication within the Clinical Project Team and with functional management.
Provides regularly updates regarding the status and progress of the trials
Manages the program(s) within the approved budgets and timelines.
Responsible for writing of clinical project deliverables such as protocols, final study report, study manuals, study tools, etc.
Directs forecasting of devices necessary for project in collaboration with supply-chain.
Supports the coordination and attends investigator and coordinator meetings, representing the clinical project team.
Provides oversight of individual clinical trials to ensure that safety concerns and/or adverse events are identified and appropriate responses to such concerns are developed and executed.
Responsible for the identification of project risks and the development and implementation of the mitigations for these risks.
Responsible for corrective action plans at individual sites and across trial. May participate in internal/external trial-related audits.
Demonstrates thorough knowledge of and coaches others in the appropriate application of clinical research conduct, laws, regulations, and standards, and compliance with applicable company’s SOPs and policies.

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