Associate Clinical Operations Manager （ACOM） / 外資製薬メーカー
|職種||Associate Clinical Operations Manager （ACOM）|
To enable AbbVie’ s emergence as a world class R D organization the position is accountable for all activities of site related study execution directly or by leadership of assigned CRAs involving start up execution and close out.
・Accountable for all activities of site related study execution of assigned studies / Monitors involving start up execution and close out. Accountable for the on time and within budget study execution of assigned projects including but not limiting to country and site feasibility.
・Oversee site evaluation/selection contracts/budget negotiation regulatory/EC submissions startup issue management relationship management monitoring and site closure. Provide local regulatory and legal requirement expertise.
・Ensure adherence to federal regulations and applicable local regulations Good Clinical Practices （GCPs） ICH Guidelines AbbVie Standard Operating Procedures （SOPs） Monitoring Plans and to quality standards in conducting clinical research. Stay abreast of new and/or evolving local regulations guidelines and policies. May monitor regulatory reforms and industry trends within country / district and provide impact analysis of significant changes affecting conduct of Clinical studies.
・Ensure audit and inspection readiness of assigned sites. Advise on pre audit activities for GCP requirements. Prepare and follow up site and system audits CAPA preparation and implementation.
・Accountable for resource management for assigned team. Provide ongoing assessment and input towards resource needs and in allocating resources in alignment with AbbVie research goals priorities and specific study timelines. Proactively identify and communicate issues impacting resource allocation and provide solutions.
・Responsible for the acquisition and retention performance management and growth and development of talent. May be responsible for being the country point of contact for CROs for an assigned study / studies. May participate/lead in global/local task forces and initiatives. Responsible for activities as assigned by manager.
・If assigned; Responsible for identifying training needs and standardizing and facilitating training solutions for SMM monitors globally. Provide consistent best practice approach to onboarding consolidating “lessons learned” across areas and incorporating into monitoring training materials defining best pra
|求める経験||・Education: Bachelors or equivalent degree health related （e.g. Medical Scientific Nursing Pharmacy） preferred
・Site Monitoring Experience: Minimum 3 years.
・Strong analytical and critical thinking skills to evaluate complex issues from multiple perspectives and drive smart decision making.
・Excellent interpersonal skills with the ability to communicate persuasively and with clarity flexibility and adaptability to changing requirements resourcefulness and creativity. Demonstrated proactive and positive team player.
・Exhibits strong planning and organizational skills and high level of flexibility in a dynamic environment with experience leading（within country） projects with competing deadlines; Experience across multiple Therapeutic Areas and Study Phases.
・Drives continuous improvement and simplicity in process and approach and enhances agility.
・Demonstrated business ethics and integrity.
|年収||900万円 - 1200万円|