🚀 Launch Your Clinical Research Career: In-House CRA (IHCRA), Japan
Join ICON plc, a world-leading healthcare intelligence and clinical research organization, as an In-House Clinical Research Associate (IHCRA) in Japan. This is your gateway to impacting clinical development, offering a vital, site-facing role where you will ensure the integrity and progress of pioneering clinical trials from our office.
We are seeking a meticulous and proactive professional to support trial management and site excellence. If you are passionate about contributing to medical innovation and excel in a collaborative, detail-oriented environment, this role is your opportunity to build a foundational career in clinical research with a global industry leader.
🎯 Your IHCRA Mission: Key Responsibilities
Trial Execution & Site Support
- Assist in the planning, initiation, and execution of clinical trial activities.
- Coordinate closely with investigative sites to ensure strict compliance with study protocols, ICH-GCP, and local regulatory requirements.
- Support remote monitoring activities, including data review and query resolution, to uphold data quality and patient safety.
- Site Feasibility & Activation
- Conduct thorough site feasibility assessments and contribute to the site selection process to ensure optimal trial placement.
- Aid in the collection, tracking, and review of essential regulatory and start-up documents for site activation.
- Progress Monitoring & Documentation
- Monitor study progress and data collection activities to ensure timelines, quality, and accuracy goals are met.
- Assist in the preparation, review, and maintenance of critical study documentation, reports, and Trial Master File (TMF) deliverables.
- Stakeholder Collaboration
- Serve as a key liaison between Clinical Research Associates (CRAs), study sites, and internal cross-functional teams.
- Facilitate clear communication to streamline processes and promptly address site or data issues.
⭐ Your Profile: IHCRA Qualifications
Essential Requirements
- Bachelor's degree in Life Sciences, Healthcare, Nursing, or a related scientific field.
- Previous experience in clinical research, a related field, or a strong academic foundation with a passion for clinical operations is preferred.
- Understanding of ICH-GCP guidelines and clinical trial processes.
- Business-level proficiency in both Japanese and English is required for effective local and international communication.
- Core Competencies
- Strong Organizational Skills: Ability to prioritize tasks effectively and manage multiple responsibilities in a fast-paced environment.
- Exceptional Attention to Detail: Meticulous approach to document review, data tracking, and compliance checks.
- Effective Communication: Excellent verbal and written skills for professional collaboration with sites and internal teams.
- Collaborative Mindset: Ability to work both independently and as part of a dynamic, international team.
💫 Why Build Your Career as an IHCRA at ICON in Japan?
Impact Clinical Development
- Play a crucial supporting role in bringing innovative treatments to patients in Japan and worldwide.
- Gain foundational experience in clinical trial conduct and site management with a leading global CRO.
- Ensure the highest standards of quality and ethics in clinical research.
- Career Growth & Development
- Structured career pathway with clear progression to field-based CRA and other clinical operations roles.
- Comprehensive training programs and ongoing mentorship from industry experts.
- Exposure to diverse therapeutic areas and complex global studies.
- Supportive & Inclusive Culture
- Join a diverse and dynamic team within ICON's collaborative global network.
- Work in an inclusive environment that values your unique perspective and fosters professional growth.
- Be part of a company dedicated to improving patient health through intelligence and innovation.
- Competitive ICON Benefits in Japan
- Attractive salary package and performance recognition.
- Comprehensive health insurance plans for you and your family.
- Generous annual leave entitlements.
- Retirement planning offerings and financial security benefits.
- Global Employee Assistance Programme (EAP) providing 24/7 confidential support.
- Flexible benefits tailored to your lifestyle, which may include commuter support, wellness programs, and more.
- Continuous professional development and training opportunities.
🌍 Your Role in Japan's Clinical Landscape
- Support trials that address both local and global health needs.
- Navigate Japan's specific regulatory and clinical research environment.
- Collaborate with leading Japanese investigative sites and healthcare professionals.
✨ Ready to Support Groundbreaking Clinical Trials in Japan?
If you are a diligent, communicative professional with a passion for clinical research and the required language skills, we encourage you to apply. This IHCRA position in Japan is the perfect platform to launch a rewarding career, ensuring the efficient and compliant progress of clinical trials that shape the future of medicine.
Apply Now and become ICON's next essential link in clinical trial excellence in Japan!
