d) - Hannover at IQVIA

Hanover, Lower-Saxony, Germany

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Not SpecifiedCompensation

Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level

Part TimeJob Type

UnknownVisa

Clinical Research, HealthcareIndustries

Requirements

At least two years of relevant experience, or an equivalent combination of medical training, education, and experience
Knowledge of clinical trials, combined with in-depth knowledge of department-, protocol-, and study-specific workflows, informed consent forms, and study plans
Strong IT skills, proficient in MS Windows and Office applications such as Access, Outlook, Excel, and Word
Excellent interpersonal skills with the ability to build and maintain effective working relationships
Very good German language skills in spoken and written form

Responsibilities

Coordinating clinical research studies and maintaining a safe study environment in accordance with health and safety guidelines under the leadership and delegation of the Principal Investigator
Ensuring patient welfare, addressing their concerns while guaranteeing the highest quality
Caring for patients and supporting staff with administrative tasks
Maintaining study protocols, case report forms (CRFs), electronic data capture systems (EDC), and other study documents up to date
Planning and coordinating logistical activities for study procedures according to the study protocol
Performing clinical preparations for the study, including labeling sample collection tubes and containers, inventorying required materials, and setting up or troubleshooting equipment and/or study issues
Data entry, verifying data quality, and responding to queries
Supporting patient enrollment in the study through recruitment, screening, and instruction according to the study protocol
Collecting, recording, and reporting clinical data and findings appropriately in CRFs and collaborating with the investigator on study-related adverse events and serious adverse events according to the study protocol
Coordinating with the study monitor on study issues and effectively answering questions raised by the monitor

Skills

Key technologies and capabilities for this role

Study CoordinationPatient CareCRF ManagementEDCData EntryPatient ScreeningAdverse Event ReportingSample LabelingInformed ConsentData Quality

Questions & Answers

Common questions about this position

What is the employment type and duration for this position?

The position is part-time, initially limited to one year, available immediately, with a scope of 40 hours per week though part-time may be possible.

Where is this job located?

The role is based at a study center in Hannover.

What skills and experience are required for this Study Nurse role?

Candidates need at least two years of relevant experience or equivalent medical training, knowledge of clinical trials and study workflows, strong IT skills in MS Windows and Office applications like Access, Outlook, Excel, and Word, and excellent interpersonal skills with very good German language proficiency.

What is the company culture like at IQVIA?

This information is not specified in the job description.

What makes a strong candidate for this Study Nurse position?

Strong candidates have at least two years of relevant experience or equivalent medical training, solid knowledge of clinical studies and workflows, proficient IT skills especially in MS Office, excellent interpersonal abilities, and very good German 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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