I

IQVIA

Runs drug trials and sells health data to pharma

Freelance Translator/Linguist - Chinese (Simplified) to English

Contract
No salary listed
Junior, Mid, Senior
Bachelor's
Melbourne VIC, Australia+1 moreMore locations: Reading, UK
In PersonOn-site work in Melbourne, Australia or Reading, United Kingdom.
Content & WritingTranslation & Interpretation

About the job

Requirements
  • Native fluency in English (target language) spoken and written
  • Fluency in Chinese (Simplified) spoken and written
  • At least 1 year of experience translating, reviewing and editing life sciences content including clinical trial documents (must be clearly outlined in CV with document types)
  • A university degree in translation or linguistics and at least 2 years of translation experience OR no university degree and at least 5 years of translation experience
  • Ability to work according to tight deadlines and independently
  • Experience with translation management systems and computer-assisted translation tools
  • All locations will be considered
  • This posting is for individual freelancers only; applications from agencies will not be accepted

About the company

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company Size

10,001+

Company Stage

IPO

Headquarters

Durham, North Carolina

Founded

1998

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Simplify's Take

What believers are saying

  • Research work is booked years ahead: IQVIA held a $34.2 billion contracted trial backlog in June 2026.
  • Big pharma is adopting its AI: 19 of the top 20 drugmakers began using IQVIA's AI agents by March 2026.
  • Headcount keeps rising: IQVIA grew from about 88,000 employees in February 2025 to 93,000 by March 2026.

What critics are saying

  • Debt limits room to invest: IQVIA carried $16 billion of debt against $1.9 billion of cash at June 30, 2026.
  • Privacy rules bite: Italy fined IQVIA's Italian unit €7 million in September 2026 for unlawfully processing 1 million patients' records.
  • Role cuts continue: IQVIA spent $105 million on restructuring, mostly severance, in 2025 and said in February 2026 cuts continue.

What makes IQVIA unique

  • Its data doubles as industry research: the IQVIA Institute publishes Global R&D Trends and Global Medicine Use Trends reports.
  • Its data reaches almost every medicine: IQVIA tracks about 90% of the world's pharmaceuticals, measured by 2024 sales.
  • A Supreme Court ruling backs its data trade: predecessor IMS Health overturned Vermont's prescriber data limits in 2011.

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Benefits

  • Health Insurance
  • Dental Insurance
  • Life Insurance
  • Flexible Work Hours
  • Paid Vacation
  • Wellness Program
  • 401(k) Retirement Plan

Growth & Insights and Company News

6 month growth

1%

1 year growth

0%

2 year growth

0%
GlobeNewswire
Oct 19th, 2026
Medera's Novoheart technology powers advanced Human Cardiac Disease Modeling at Singapore's new CIPHER research centre.

Medera's Novoheart technology powers advanced Human Cardiac Disease Modeling at Singapore's new CIPHER research centre. October 19, 2026 08:00 ET | Source: Medera Inc. National Heart Centre Singapore's new research centre integrates Novoheart's proprietary Heart-in-a-Jar technology with patient-derived cardiac disease models to advance cardiovascular research and drug discovery Collaboration expands Novoheart's international footprint, building on technology deployment at University Medical Center Utrecht and AstraZeneca, pharmaceutical collaborations, and its strategic partnership with IQVIA BOSTON and SINGAPORE, Oct. 19, 2026 (GLOBE NEWSWIRE) - Medera Inc. ("Medera"), a clinical-stage biotechnology company developing disease-modifying gene therapies for cardiovascular diseases, today announced that its wholly owned preclinical subsidiary, Novoheart, is contributing its proprietary human cardiac technologies to the newly launched Centre for Integrative Human Cell Research and Translation (CIPHER) at the National Heart Centre Singapore (NHCS). Officially launched on October 16, 2026, during the 6th NHCS Heart to Heart Gala at The Ritz-Carlton, Millenia Singapore, CIPHER represents an important initiative to advance human-relevant cardiovascular disease modeling and translational drug discovery. The launch was launched by Singapore's Senior Minister of State, Mr. Tan Kiat How. CIPHER is the first centre in the Asia-Pacific region dedicated to cardiovascular stem cell research and translational drug discovery using human heart cells derived from blood samples of Asian patients. The centre builds upon NHCS's extensive collection of more than 40 patient-derived cardiac disease models, including models of heart failure, arrhythmogenic disorders, and cardiomyopathies. By generating induced pluripotent stem cells from patient samples and differentiating them into functional human heart cells, researchers can investigate disease mechanisms and potential therapeutic responses in a patient-relevant context. Advancing Human Cardiac Disease Modeling Through Novoheart's Proprietary Technologies Novoheart is a pioneer in human cardiac tissue engineering, with more than two decades of research and development spanning individual human cardiomyocytes, engineered cardiac tissues, and functional human ventricular chamber models. Its proprietary Human Heart-in-a-Jar(TM) technology is a miniaturized, bioengineered human ventricular chamber capable of generating pressure and ejecting fluid, reproducing key physiological characteristics of the human heart in a controlled laboratory environment. Unlike conventional cell- and tissue-based assays, the Heart-in-a-Jar enables researchers to measure physiologically complex and clinically relevant parameters of cardiac pump performance, including cardiac output, ejection fraction, stroke volume, stroke work, and pressure-volume relationships. These integrated chamber-level measurements cannot be obtained from conventional isolated-cell assays and provide an important functional bridge between laboratory-based disease modeling and clinical assessment. Within CIPHER, Novoheart's technologies will complement NHCS's patient-derived disease models by extending investigations across multiple levels of human cardiac biology, from individual cells to functional engineered cardiac tissues and chambers. CIPHER's research approach integrates four dimensions of cardiac biology: mechanical function, electrical activity, cellular metabolism, and tissue organization. The combination of these capabilities is intended to support more comprehensive investigations of cardiovascular disease mechanisms and the evaluation of potential therapeutic approaches. By combining patient-specific disease biology with advanced measurements of integrated cardiac function, the collaboration aims to improve the physiological relevance and predictive potential of human-based preclinical cardiovascular research. Expanding Novoheart's International Technology Footprint The collaboration with NHCS builds upon Novoheart's growing international presence and its strategy to make advanced human cardiac technologies more broadly accessible to academic researchers, pharmaceutical companies, and biotechnology developers. Novoheart's proprietary CTScreen(TM) human cardiac tissue screening platform has been deployed at leading academic and pharmaceutical research institutions, including University Medical Center Utrecht in the Netherlands and AstraZeneca in Sweden, supporting applications in cardiac disease modeling, therapeutic screening, and translational cardiovascular science. Novoheart has also collaborated with leading global pharmaceutical companies, including Pfizer and Amgen, on applications of its human cardiac technologies in preclinical research and drug development. More recently, Novoheart established a strategic partnership with IQVIA aimed at expanding access to its human-specific cardiac disease modeling and drug discovery platforms through IQVIA's international laboratory infrastructure and pharmaceutical industry relationships. This collaboration represents an important step toward broader international deployment and commercial adoption of Novoheart's technologies. Beyond external research and pharmaceutical collaborations, Novoheart's human mini-Heart technology platform has generated preclinical human data supporting the successful FDA IND and Fast Track designation applications for ongoing gene therapy clinical trials for heart failure by Sardocor, Medera's clinical-stage subsidiary. Together, these initiatives demonstrate Novoheart's growing role in bridging human-based preclinical research and clinical drug development. This strategy aligns with the increasing emphasis on human-relevant, non-animal approaches to preclinical drug development, as reflected in the FDA Modernization Act 2.0. Leadership Perspective "For more than two decades, we have pioneered the development of human cardiac models, progressing from individual heart cells to functional engineered human heart tissues and chambers," said Ronald Li, PhD, Chairman and Chief Executive Officer of Medera. "Our Heart-in-a-Jar technology represents an important advance in human cardiac disease modeling by enabling researchers to measure clinically relevant parameters of cardiac pump function, such as cardiac output and ejection fraction, in a laboratory setting. These capabilities bring us closer to studying human cardiac physiology and disease in ways that are directly relevant to clinical medicine." "Our collaboration with NHCS brings together Novoheart's proprietary technologies with extensive patient-derived disease models and clinical expertise. Alongside our expanding international collaborations with leading academic institutions and pharmaceutical partners, we believe this initiative will help accelerate the adoption of more predictive, human-relevant approaches to cardiovascular research and drug discovery." About Medera Inc. Medera is a clinical-stage biotechnology company developing next-generation gene therapies for cardiovascular and other serious diseases. Its pipeline includes multiple adeno-associated virus (AAV)-based gene therapy programs targeting heart failure and related cardiovascular disorders. The Company operates through two complementary business units: Novoheart, which develops advanced human-specific cardiac disease modeling and drug discovery platforms, and Sardocor, which leads clinical development of Medera's gene therapy pipeline. Together, these capabilities create an integrated translational platform spanning drug discovery, preclinical validation, manufacturing, and clinical development. About Novoheart Novoheart is a pioneer in human cardiac tissue engineering and develops proprietary human-specific platforms for cardiac disease modeling, drug discovery, and preclinical evaluation. Its technologies include engineered human cardiac tissues, electrophysiological screening systems, and ventricular chamber models, including its proprietary Human Heart-in-a-Jar(TM) platform. The Heart-in-a-Jar enables researchers to investigate integrated cardiac pump function through physiologically complex measurements, including cardiac output, ejection fraction, stroke volume, and pressure-volume relationships, complementing conventional cellular and tissue-based assays. Novoheart's platforms support investigations of cardiac physiology, disease mechanisms, drug responses, and potential cardiotoxicity using human-relevant, non-animal experimental systems. Through collaborations with leading academic research institutions and pharmaceutical industry partners, Novoheart is advancing the international deployment and commercialization of its human cardiac technologies. Forward-Looking Statements This press release contains forward-looking statements regarding Medera's and Novoheart's anticipated research activities, strategic collaborations, technology deployment, international expansion, commercialization opportunities, and potential applications of their proprietary platforms. These statements are based on current expectations and involve risks and uncertainties that may cause actual results to differ materially from those expressed or implied. Such risks include uncertainties relating to the establishment and operation of new facilities, execution of research collaborations, development and deployment of technologies, commercialization activities, regulatory developments, and other factors affecting the Company's business and operations. Forward-looking statements speak only as of the date of this release. Medera undertakes no obligation to update these statements except as required by applicable law. Stephanie Carrington Investor Relations ICR Healthcare [email protected] 646.277.1282

BioPharma Watch
Oct 7th, 2026
IQVIA launches IQVIA Explorer to help life sciences companies make better commercial decisions.

IQVIA launches IQVIA Explorer to help life sciences companies make better commercial decisions. Key Takeaway: IQVIA has launched IQVIA Explorer at TechIQ 2026, aimed at assisting life sciences companies in making informed commercial decisions. This new tool enables users to convert complex analytics projects into a continuous commercial intelligence resource. It allows for the application of external indicators to address business questions effectively. Market sentiment analysis. Positive factors. * Launch of IQVIA Explorer enhances decision-making for life sciences companies. * Provides an always-on commercial intelligence capability. * Transforms complex analytics into user-friendly insights. RESEARCH TRIANGLE PARK, N.C.-(BUSINESS WIRE)-IQVIA (NYSE:IQV), a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries, today at TechIQ 2026 introduced IQVIA Explorer(TM) to help customers make better-informed commercial decisions. IQVIA Explorer turns complex, one-time analytics projects into an always-on commercial intelligence capability. Users can apply external indicators and ask business questio Frequently asked questions. What is IQVIA Explorer? IQVIA Explorer is a new tool designed to help life sciences companies make informed commercial decisions. When was IQVIA Explorer launched? IQVIA Explorer was launched at TechIQ 2026. How does IQVIA Explorer assist users? It transforms complex analytics projects into an always-on commercial intelligence capability. What industries does IQVIA serve? IQVIA provides services to the life sciences and healthcare industries.

BioPharma Watch
Oct 7th, 2026
IQVIA launches IQVIA Life Science Models to help life sciences companies predict clinical trial outcomes.

IQVIA launches IQVIA Life Science Models to help life sciences companies predict clinical trial outcomes. Key Takeaway: IQVIA has launched the IQVIA Life Science Models at TechIQ 2026, designed to assist life sciences companies in predicting clinical trial outcomes. This suite of models integrates proprietary content and extensive regulatory knowledge, aiming to improve decision-making in clinical research. The initiative reflects IQVIA's commitment to advancing healthcare intelligence. Market sentiment analysis. Positive factors. * Launch of innovative IQVIA Life Science Models. * Models aim to enhance prediction of clinical trial outcomes. * Combines expert content and regulatory knowledge. RESEARCH TRIANGLE PARK, N.C.-(BUSINESS WIRE)-IQVIA (NYSE:IQV), a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries, today at TechIQ 2026 introduced IQVIA Life Science ModelsTM to help predict clinical trial outcomes. IQVIA Life Science Models are a suite of purpose-built models for life sciences, combining IQVIA's proprietary expert content, deep domain knowledge and established regulatory, com Frequently asked questions. What are IQVIA Life Science Models? IQVIA Life Science Models are a suite of models designed to predict clinical trial outcomes. When were the IQVIA Life Science Models launched? The models were launched at TechIQ 2026. What does the IQVIA Life Science Models integrate? They combine proprietary expert content and deep regulatory knowledge. Who can benefit from IQVIA Life Science Models? Life sciences companies looking to enhance their clinical trial predictions can benefit.

IQVIA Holdings Inc.
Oct 7th, 2026
IQVIA launches IQVIA Life Science Models to help life sciences companies predict clinical trial outcomes.

IQVIA launches IQVIA Life Science Models to help life sciences companies predict clinical trial outcomes. 10/07/2026 RESEARCH TRIANGLE PARK, N.C.-(BUSINESS WIRE)- IQVIA (NYSE:IQV), a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries, today at TechIQ 2026 introduced IQVIA Life Science Models(TM) to help predict clinical trial outcomes. IQVIA Life Science Models are a suite of purpose-built models for life sciences, combining IQVIA's proprietary expert content, deep domain knowledge and established regulatory, compliance and privacy frameworks. Built using technologies including NVIDIA Nemotron(TM) and supported by Amazon Web Services (AWS) infrastructure, the models connect molecular and treatment information with patient journeys and clinical outcomes to enable predictive applications across clinical development. * Clinical study simulation and protocol optimization, including endpoint selection, patient eligibility criteria, dose selection and sample size planning, helping teams identify risks before trials begin. In initial evaluation across 50 trials and 270 endpoints, 85% of predictions were on target or clinically close. * Digital twins and synthetic controls that support more efficient study designs. * Leverage clinical study predictions to inform better real-world planning and access. In clinical development, Life Science Models extend IQVIA's Predictive Clinical Development approach, enabling sponsors to simulate studies and test key assumptions before execution, helping optimize study design and identify potential risks earlier. About IQVIA IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA's portfolio of solutions are powered by IQVIA Connected Intelligence(TM) to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI(R), advanced analytics, the latest technologies and extensive domain expertise. IQVIA is committed to using AI responsibly, with AI-powered capabilities built on best-in-class approaches to privacy, regulatory compliance and patient safety, and delivering AI to the high standards of trust, scalability and precision demanded by the industry. With approximately 94,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA's insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures. To learn more, visit www.iqvia.com. Kerri Joseph, IQVIA Investor Relations ([email protected]) +1.973.541.3558 Multimedia Files: Company's logo

Daily AI Tools
Oct 5th, 2026
IQVIA fined $7.8 million for failing to properly anonymize health data.

IQVIA fined $7.8 million for failing to properly anonymize health data. By Bill Toulas Monday, October 5, 2026 BleepingComputer Italy's data regulator fined IQVIA $7.8 million for failing to properly anonymize the medical records of one million patients. This enforcement highlights a critical flaw in health-tech security: "pseudonymized" data often remains identifiable. For the industry, it serves as a stark warning that GDPR compliance require BleepingComputer