IQVIA Service at IQVIA

Tokyo, Japan

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Life Sciences, PharmaceuticalsIndustries

Requirements

Bachelor’s degree in Life Sciences or a related field
At least 8 years of experience in medical writing
At least 3 years of experience in line management
Deep knowledge of clinical trial-related documents (e.g., Clinical Trial Protocol, Clinical Study Report, Common Technical Document)
Ability to review statistical analysis plans and identify statistical output errors and inconsistencies
Ability to integrate, interpret, and summarize data from various sources
Team management and leadership skills
Problem-solving skills
Project management skills (planning, organization, and multitasking)
Judgment, negotiation, decision-making, and problem-solving abilities
Business acumen and financial analysis skills, strategic planning, and budgeting

Responsibilities

Lead the creation of various documents
Provide advice to team members on document creation and customer requirements
Manage project deliverables, including timeline, scope, quality, and revenue
Lead daily customer interactions within projects
Manage project plans (timeline, deliverables, scope, quality, revenue)
Conduct regular meetings with direct reports to discuss project status, schedule, budget risks, team productivity, SOP compliance, and career development
Implement activities to maintain team engagement
Collaborate with the sales team to prepare customer proposals
Build and maintain good relationships with other IQVIA internal departments
Review statistical analysis plans and identify statistical output errors and inconsistencies
Integrate, interpret, and summarize data from various sources

Skills

Key technologies and capabilities for this role

Medical WritingClinical Trial ProtocolClinical Study ReportCommon Technical DocumentStatistical Analysis PlansProject ManagementTeam ManagementLeadershipData IntegrationData InterpretationBudgetingStrategic Planning

Questions & Answers

Common questions about this position

What experience is required for this Lead Medical Writer position?

Candidates need at least 8 years of experience in medical writing, including 3 years in line management, a Bachelor’s degree in Life Sciences or related field, and deep knowledge of clinical trial-related documents like Clinical Trial Protocol and Clinical Study Report.

What key skills are needed for this role?

Essential skills include reviewing statistical analysis plans to identify errors, integrating and summarizing data from various sources, team management and leadership, project management, problem-solving, and business acumen with financial analysis.

Is this position remote or does it require office work?

This information is not specified in the job description.

What is the salary or compensation for this role?

This information is not specified in the job description.

How can I stand out when applying for this position?

Highlight your 8+ years in medical writing with 3+ years in management, expertise in clinical documents and statistical review, plus strong leadership, project management, and data integration skills to demonstrate fit for leading teams and projects.

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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