Clinical Trials Assistant (CTA) (Evergreen) at IQVIA

Hong Kong

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical ResearchIndustries

Requirements

High School Diploma or equivalent
3 years of administrative support experience
Computer skills: Microsoft Word, Excel, and PowerPoint
Written and verbal communication skills (good command of English)
Time management and organizational skills
Ability to establish and maintain effective working relationships
Awareness of applicable clinical research regulatory requirements (GCP and ICH guidelines)
Knowledge of applicable protocol requirements

Responsibilities

Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF))
Assist with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports
Assist with periodic review of study files for completeness
Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information
Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation
May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training

Skills

Key technologies and capabilities for this role

Microsoft WordMicrosoft ExcelMicrosoft PowerPointGCPICH guidelinesTMF managementTime managementOrganizational skillsEnglish communicationClinical protocol knowledge

Questions & Answers

Common questions about this position

What is the salary for the Clinical Trials Assistant position?

This information is not specified in the job description.

Is this a remote position or is there a required location?

This information is not specified in the job description.

What skills are required for the Clinical Trials Assistant role?

Required skills include computer skills in Microsoft Word, Excel, and PowerPoint; written and verbal communication skills with good command of English; time management and organizational skills; ability to establish and maintain effective working relationships; awareness of GCP and ICH guidelines; and knowledge of protocol requirements.

What is the company culture like at IQVIA?

This information is not specified in the job description.

What qualifications make a strong candidate for this Clinical Trials Assistant role?

A strong candidate will have a High School Diploma or equivalent, 3 years of administrative support experience, proficiency in Microsoft Office tools, strong communication and organizational skills, and awareness of clinical research regulations like GCP and ICH guidelines.

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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