Clinical Trial Assistant at IQVIA

Reading, England, United Kingdom

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Life Sciences, Clinical Research, PharmaceuticalsIndustries

Requirements

Awareness of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Knowledge of applicable protocol requirements
Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
Good written and verbal communication skills including excellent command of English
Effective time management and organizational skills
Ability to establish and maintain effective working relationships with coworkers, managers and clients

Responsibilities

Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines
Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures
Assist with periodic review of study files for completeness
Assist CRAs/iCRAs 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 and with required approval
May perform assigned administrative tasks to support team members with clinical trial execution

Skills

Key technologies and capabilities for this role

Clinical Trial ManagementClinical SystemsSite Compliance TrackingClinical DocumentationCRF ManagementClinical Data FlowRegulatory DocumentationClinical Trial Supplies

Questions & Answers

Common questions about this position

Is this role remote or does it require office presence?

This role requires frequent travel to Luton and is not remote.

What skills are required for the Clinical Trial Assistant position?

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

What is the salary or compensation for this role?

This information is not specified in the job description.

What is the company culture like at IQVIA?

IQVIA advocates for diversity and inclusion in the workplace, believing it provides a competitive advantage in the global marketplace.

What should I know before applying for this Clinical Trial Assistant role?

This role is not eligible for UK visa sponsorship, requires frequent travel to Luton, and demands knowledge of GCP/ICH guidelines and strong organizational skills.

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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