Site Research Assistant - Den Bosch at IQVIA

Utrecht, Utrecht, Netherlands

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Part TimeJob Type

UnknownVisa

Clinical Research, HealthcareIndustries

Requirements

BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting (e.g., clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession)
At least 1-2 years experience working as a Clinical Research Assistant or Clinical Research Coordinator at a clinical trial site
Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
Basic knowledge of medical terminology
Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers, and clients
Good organizational skills with the ability to pay close attention to detail

Responsibilities

Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
Support with screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.)
Planning and coordinating logistical activity for study procedures according to the study protocol
Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
Management and shipment of biological samples
Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions
Supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator
Involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial
Administrative research tasks

Skills

Key technologies and capabilities for this role

Clinical TrialsEDC SystemsCRF ManagementPatient ScreeningInformed ConsentData EntryQuery ResolutionBiological Sample ManagementStudy ProtocolsLogistics Coordination

Questions & Answers

Common questions about this position

Is this a full-time or part-time position?

This is a part-time position requiring 24 hours per week, expected to last around 6 months with an immediate start.

What is the salary or compensation for this role?

This information is not specified in the job description.

What qualifications and skills are required for this position?

Candidates need a BS/BA in life sciences or equivalent with 1-2 years experience as a Clinical Research Assistant or Coordinator, good knowledge of clinical trials, basic medical terminology, strong IT skills in MS Office, and excellent interpersonal and organizational skills.

What does the team structure look like for this role?

The role is part of the site team, working under the direction and delegation of the Principal Investigator while supporting the clinical trial team.

What makes a strong candidate for this Research Assistant role?

A strong candidate will have 1-2 years of direct experience as a Clinical Research Assistant or Coordinator in a clinical trial site, combined with a life sciences background, clinical trials knowledge, IT proficiency, and strong organizational and interpersonal 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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