安全性情報管理部門ラインマネージャー (Pharmacovigilance Line Manager) at IQVIA

Tokyo, Japan

IQVIA Logo
Not SpecifiedCompensation
Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level
Full TimeJob Type
UnknownVisa
CRO, Pharmaceuticals, Healthcare, Medical DevicesIndustries

Requirements

  • Experience in case management related to safety information management for pharmaceuticals and medical devices
  • Experience in improving quality and productivity in case processing operations
  • Experience in personnel management/guidance, such as as a manager, leader, mentor, or trainer
  • Business-level Japanese proficiency (reading, writing, and conversation)
  • Business-level English proficiency (reading and writing)
  • Business-level proficiency in MS Office, especially Excel for simple data aggregation and calculations
  • Ability to build good relationships with clients, other departments, and team members

Responsibilities

  • Perform line management for a team of 10-20 people through staffing plans, task allocation, and task guidance
  • Achieve and maintain a supportive and comfortable work environment through regular communication with team members
  • Conduct performance evaluations and career development for members
  • Collaborate with other managers to schedule projects, plan staffing, predict peak workloads, and confirm, evaluate, and report on project status
  • Lead continuous improvements in the team's work processes, procedures, and infrastructure
  • Monitor and lead improvements in deliverables' quality, timelines, costs, and productivity
  • Identify members' training needs and develop and implement training plans

Skills

Key technologies and capabilities for this role

PharmacovigilanceCase ManagementCase ProcessingTeam ManagementExcelMS OfficeArgusQuality ImprovementProductivity ImprovementProject SchedulingResource PlanningPerformance Evaluation

Questions & Answers

Common questions about this position

What is the work arrangement and location for this role?

The position follows a Flexible Style Work policy with a main focus on working from home, and office attendance at Shinagawa HQ or Shin-Osaka as needed.

What are the required qualifications for this position?

Must have experience in safety information management for pharmaceuticals/medical devices including case management, quality/productivity improvement in case processing, people management/mentoring experience, business-level Japanese (all skills), business-level English (reading/writing), MS Office proficiency especially Excel for data aggregation, and ability to build good relationships.

What does the salary and compensation look like?

Salary is determined according to company regulations with favorable treatment, includes raises and bonuses, but no overtime allowance as it is a management position.

What benefits are offered in this role?

Comprehensive welfare benefits include both statutory social insurance and IQVIA's own unique programs, flex time, remote work system, passive smoking measures, and various holidays such as annual paid leave, summer vacation, sick leave, special leave, women's special leave, childcare/caregiving leave, and nursing leave.

What is the team size and management responsibilities?

The role involves line management of a team of approximately 10-20 members, including staffing plans, task allocation, guidance, regular communication for a supportive environment, performance evaluation, career development, process improvements, quality monitoring, and training plans.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters
1998Year Founded
$3,526MTotal Funding
POST_IPO_EQUITYCompany Stage
Cybersecurity, Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.
Proliferation of disparate technological solutions causes technology overload in clinical trials.
Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.
The company offers privacy-enhancing technologies to protect individual patient data.
IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.
AI-driven drug discovery accelerates identification of potential drug candidates.
Expansion of telemedicine facilitates remote patient monitoring and data collection.

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