Clinical Research Coordinator - Gozée at IQVIA

Brussels, Brussels, Belgium

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Part TimeJob Type

UnknownVisa

Clinical Research, HealthcareIndustries

Requirements

Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)
Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
Good knowledge of medical terminology
Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
At least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
Excellent interpersonal and communication skills
Strong organizational skills and attention to detail
Fluency in French and good command of English

Responsibilities

Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems
Supporting patient screening and enrollment, including handling informed consent and privacy documentation
Coordinating logistical activities for study procedures in line with the study protocol
Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
Managing and shipping biological samples
Communicating with study monitors and responding to study-related inquiries
Helping with patient recruitment, patient education and community outreach
Carrying out general administrative tasks related to the study

Skills

Key technologies and capabilities for this role

Clinical TrialsStudy ProtocolsInformed ConsentEDC SystemsCRFsData EntryPatient ScreeningSample ManagementMS OfficeExcelMedical Terminology

Questions & Answers

Common questions about this position

Is this a full-time or part-time position, and how many hours per week?

This is a part-time position requiring 15 hours per week.

What is the duration and start date for this role?

The position starts immediately and has an approximate duration of 6 months.

What education and experience are required for this Clinical Research Coordinator role?

A Bachelor’s degree in life sciences or equivalent is required, along with 1-2 years of experience as a Clinical Research Assistant, Research Nurse, or Clinical Research Coordinator at a clinical trial site, plus relevant experience in a clinical or medical setting.

What key skills are needed for this position?

Candidates need a solid understanding of clinical trials, good knowledge of medical terminology, strong IT skills including MS Office proficiency, excellent interpersonal and communication skills, strong organizational skills, attention to detail, and fluency in French with good English command.

What is the work environment like at IQVIA?

You will join a global team in a collaborative and dynamic environment that advances healthcare through data, technology, and human science, with supportive work settings and impactful 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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