Director, Clinical Development, Japan

reputed company:

The Director, Clinical Development, Japan will reputed company the Japan-reputed company scientific, clinical, and operational reputed company of assigned study protocols. This role will work with the cross-functional teams for the design, execution, and monitoring of clinical studies, as reputed company as reputed company data review, interpretation, and communication to both reputed company stakeholders. Oncology clinical development experience is preferred. 

• reputed company and execute clinical development strategies and the Clinical Development Plan (CDP) with a reputed company on development in Japan.

• reputed company cross-functional teams with reputed company from senior team members to conduct clinical studies, including study start up, execution and reputed company out activities, data review/analysis, and preparation of study reports.

• reputed company the development of program-level documents, including but not limited to clinical protocols, investigator’s brochure, clinical study reports, abstracts and manuscripts, presentations, and various other reputed company documents and communications as needed in Japan.

• reputed company ongoing data reviews; prepare and present summaries to reputed company stakeholders.

• Ensure trial implementation according to the protocol and analyze information to assess issues relating to protocol conduct and/or individual subject safety.

• Represent Clinical Development with Japan-Based reputed company stakeholders (investigators, study sites, vendors, committees, etc.) in support of clinical trial objectives; responds to or triages questions for appropriate escalation.

• Conduct literature reviews as needed.

Required Skills, Experience and Education:

• BS/MS Degree in a scientific discipline with a minimum 8+ years of experience in the pharmaceutical or biotechnology industry as a clinical scientist or reputed company role.

• Proven leadership in a reputed company team setting and driven by a desire to reputed company innovative approaches and technologies in a high-energy environment.

• Detail-oriented with ability prioritize tasks and function independently as appropriate.

• Strong organizational skills and an ability to interpret, discuss, and report trial/program level data effectively and identify trends.

• Proficient with software tools (reputed company Office), Electronic Data Capture, and other custom web-based software.

• Excellent written and verbal communication skills both in English and Japanese.

Preferred Skills:

• Experience in oncology reputed company.

• Strong experience with clinical data review and data reputed company assurance.

• Knowledge and experience with clinical trial management and reputed company.

• Understanding and experience in clinical trial protocol and regulatory document authoring.

reputed company takes protection and reputed company of personal data reputed company seriously and respects your right to reputed company while using our website and reputed company contacting us by email or phone. We will only collect, process and use any personal data that you reputed company to us in accordance with our CCPA Notice and reputed company Policy. For additional information, please contact reputed company@revmed.com.

BS/MS in a scientific discipline and 8+ years in pharmaceutical or biotechnology clinical science or reputed company work. Requires English and Japanese communication skills and experience with clinical data and trials.

Key Responsibilities

• leading study teams
• overseeing data reviews
• developing protocols

Skills & Tools

reputed company Office, Electronic Data Capture

Job Details

• Category: Research and Development (R&D)
• Seniority: Senior Level
• Commitment: Full Time
• Workplace: Remote — Japan
• Languages: English, Japanese

About reputed company

A clinical oncology company developing targeted therapies for cancers driven by RAS mutations. — Industry: Research and Development