Senior Clinical Research Associate (CRA)
Location: Japan (Osaka) On-site
About Us:
Deep Intelligent Pharma (DIP
) is one the fastest growing and well-funded AI companies. It 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, scale, and scientific excellence. Founded in 2017, DIP is not just digitizing existing processes; we are fundamentally reimagining how drugs are discovered and developed. Our next-generation platform, built in partnership with Microsoft and Google, harnesses multi-agent AI swarms to perform scientific writing, data management, statistical reasoning, clinical programming, and regulatory compliance with superhuman precision. Trusted by over 1,000 global pharmaceutical companies and biotechs, we are at the forefront of fusing AI with life science innovation. Notable investors includes Sequoia and SIG.
Website :
Job Responsibilities:
1.
Requirements analysis and solution development
: Conduct in-depth analysis of client needs, independently design clinical trials and system solutions, and assist with project quotations.
2.
Overall project management
: Develop full-cycle project plans, coordinate cross-departmental resources, manage progress and quality, and ensure on-time project delivery.
3.
Client communication and relationship management
: Regularly report project progress, efficiently resolve implementation issues, and enhance client satisfaction.
4.
Quality and documentation management
: Supervise Standard Operating Procedure (SOP) execution and document compliance, ensuring the entire process is traceable and without omissions.
- T
eam building and process optimization
: Build a project manager pipeline and conduct professional training. Participate in the standardization of departmental systems and procedures.
Qualifications:
Bachelor's degree or above in Clinical Medicine, Pharmacy, or related majors, with 8+ years of work experience, including 5 years of project management experience in clinical research or healthcare systems.
Proficient in independently designing clinical trial protocols; familiar with new drug R&D processes and cutting-edge industry technical standards.
Good reading, comprehension, and writing skills in Japanese or English, as well as fluent oral expression skills; proficient in the Microsoft Office suite.
Clear logical thinking, with excellent copywriting skills, cross-departmental negotiation skills, and complex problem-solving abilities.
Goal-oriented leadership, skilled in team empowerment and process optimization, and able to adapt to a high-intensity collaborative environment.
To Apply
: Please submit your resume and a brief cover letter outlining your experience in the pharmaceutical industry and your passion for the potential of AI to transform clinical development. Please email your resume to
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