Clinical Research Coordinator III – RN
Thermo Fisher ScientificSalary not specified
Part Time
Senior (5 to 8 years), Expert & Leadership (9+ years)
Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Part TimeJob Type
UnknownVisa
Klinische Forschung, Pharma, GesundheitswesenIndustries
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, 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
- Coordination and organization of clinical study processes
- Ensuring a safe study environment in accordance with health and safety guidelines
- Care and support of patients
- Maintenance of study documents (CRFs, EDC systems) and data quality
- Planning and organization of logistical processes according to the study protocol
- Support in patient recruitment, screening, and briefing
- Collaboration with the principal investigator and study monitor on study-related topics
Skills
Klinische Studien
Patientenbetreuung
CRFs
EDC-Systeme
MS Office
Excel
Word
Access
Outlook
Protokollmanagement
Screening
Rekrutierung
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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