Studienassistenz / Study Nurse (m/w/d) - Hannover at IQVIA

Hanover, Lower-Saxony, Germany

IQVIA Logo
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

Study Coordination
Patient Care
CRF Management
EDC
Data Entry
Patient Screening
Adverse Event Reporting
Sample Labeling
Informed Consent
Data Quality

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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