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AbbVie

Global biopharmaceutical company developing medicines

Medical Operation Manager

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeMinato City, Tokyo, JapanNo salary listedHybrid

About the Job

Requirements

  • Be familiar with GPSP and GCP guidelines and local regulatory regulations.
  • Have knowledge of applicable study regulations and AbbVie compliance policies.
  • Develop and maintain product and scientific knowledge through textbooks, journal articles, and relevant scientific updates.
  • Be prepared to travel to relevant locations when required.
  • Adapt to changing or new work conditions and requirements.

Responsibilities

  • Conduct and manage post-marketing surveillance (PMS) for drugs and medical devices, including vendor oversight and reporting.
  • Take overall responsibility for planning, implementation, and communication of PMS in accordance with GPSP requirements.
  • Manage post-marketing surveillance with on-site and off-site vendors.
  • Plan and implement required GPSP training for relevant employees and others as appropriate.
  • Implement corrective actions when necessary after self-inspection.
  • Educate PMS members, including on-site vendors, about GVP and GPSP knowledge.
  • Act as the post-marketing surveillance manager for drugs and medical devices in relation to PMS activity.
  • Manage Medical Affairs-initiated company-sponsored study projects.
  • Identify and manage vendors to conduct each study.
  • Manage and track investigator-initiated studies requested by healthcare professionals.
  • Communicate closely with Medical Advisors and MSLs to plan and conduct studies smoothly.
  • Communicate closely with PV and PMQA representatives to support safety information related to aesthetics products.
  • Manage vendors to maintain effective relationships in terms of cost and outcomes.
  • Work closely with the Country Medical Director to track expenses against budget and report monthly variations.
  • Collaborate effectively with other Medical Affairs functions, global counterparts, and vendors.
  • Ensure study-related activities comply with AbbVie compliance policies and global and local study implementation regulations.
  • Educate cross-functional counterparts about applicable regulations.
  • Assess performance levels, identify root causes, and develop action plans for continuous improvement in areas of responsibility.
  • Apply knowledge and skills gained in AbbVie training programs to work practices and follow up.
  • Participate and work in events including congresses, symposia, field visits, and training programs.
  • Take responsibility for company projects.

About the Company

AbbVie

Global biopharmaceutical company developing medicines

AbbVie is a global biopharmaceutical company that develops and sells medicines to treat serious health conditions. Its portfolio spans immunology, oncology, virology, neuroscience, and aesthetics, with products designed to modulate the immune system, target disease pathways, or support medical aesthetics. AbbVie compounds its products through a heavy emphasis on research and development, investing billions to build a steady pipeline of new therapies. Its medicines are brought to market by selling to healthcare providers, hospitals, and clinics, and in some cases directly to patients via prescriptions. The company differentiates itself through a wide, globally distributed product line, substantial R&D investment, and a commitment to sustainability and patient care, including science-based targets. AbbVie’s goal is to improve patient outcomes by delivering effective treatments for unmet medical needs while pursuing long-term, responsible growth across healthcare markets.

Company size
10,001+
Company stage
IPO
Headquarters
North Chicago, IL
Founded
1888

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