Assoc Medical Writer (契約社員） at IQVIA

Tokyo, Japan

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, Life Sciences, HealthcareIndustries

Requirements

Preferably graduated from a science-related university
Experience in QC of clinical trial-related documents (CSR, CTD) is preferred
Experience in editing and QC of Japanese documents is acceptable
Experience in editing and QC of English documents is acceptable
Basic knowledge of clinical trials
Ability to perform document consistency checks using Word
Ability to unify terminology within documents and confirm consistency with analysis results, figures, and tables
Proficiency in handling documents such as PDF and Word
Cooperativeness as a team member to achieve results
Ability to complete tasks within specified timelines

Responsibilities

Edit and perform QC on documents created in clinical trials, PMS, and clinical research
Comply with internal SOPs or client SOPs and complete tasks within specified timelines
Seek support from experienced staff as needed and engage in appropriate communication
Edit and QC documents created by medical writers
Complete tasks within specified timelines
Cooperate as a team member to contribute to high-quality document creation

Skills

Key technologies and capabilities for this role

Microsoft WordDocument QCCSRCTDClinical TrialsSOP ComplianceJapanese EditingEnglish EditingPDF HandlingTerm Consistency

Questions & Answers

Common questions about this position

What is the employment type and contract duration for this position?

This is a full-time contract position with a 1-year contract anticipated, renewed annually.

Is remote work available for this role?

Yes, the position is planned as remote work.

What skills are required for this Associate Medical Writer role?

Required skills include basic knowledge of clinical trials, ability to perform document consistency checks using Word, confirming terminology uniformity and consistency with analysis figures/tables, proficiency with PDF and Word documents, teamwork and cooperation, and meeting deadlines.

What experience is preferred for this position?

A science university degree is desirable. Experience with QC of clinical trial documents (CSR, CTD), editing/QC of Japanese documents, or editing/QC of English documents is preferred.

What does the team environment look like at IQVIA for this role?

The role involves working as a team member to cooperate on high-quality document creation, supporting experienced staff as needed, and maintaining appropriate communication while adhering to SOPs and timelines.

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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