Virtual Trials - Clinical Research Coordinator
IQVIA
Prague, Czechia
před 7 hodinami

IQVIA Virtual Trials brings studies directly to patients wherever they are as 100% remote studies or as hybrids blending patient-centric approaches with traditional site-based elements.

Our decentralized model offers the adaptability necessary to meet any sponsor’s requirements small or large, local or global."

Job Summary

As a Virtual Trial Clinical Research Coordinator, you will perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and / or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP).

Assist with daily workload planning.

Responsibilities

  • Provide clinical research support to investigators to prepare for and execute assigned research studies, including :
  • Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data;
  • Attend all relevant study meetings;
  • Collect and submit regulatory / ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research;
  • Recruit and screen patients for clinical trials and maintain subject screening logs;
  • Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits;
  • Design and maintain source documentation based on protocol requirements;
  • Schedule and execute study visits and perform study procedures;
  • Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness;
  • Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics;
  • Monitor subject safety and report adverse reactions to appropriate medical personnel;
  • Correspond with research subjects and troubleshoot study-related questions or issues;
  • Participate in huddles to confirm daily study tasks are assigned to team members and are executed to the expected standards;
  • Assist with study data quality checking and query resolution.
  • Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring.
  • Record, report and interpret study findings appropriately to develop a study-specific database.
  • Experience

  • Typically requires a minimum of 2 - 5 years of experience.
  • 3 years’relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician;
  • or equivalent combination of education, training and experience

    Physical Demands

    Use hands and fingers to handle and manipulate objects and / or operate equipment - Frequently

    Perform unaided lifting of objects, please list the amount of weight that would be lifted, along with the frequency required - Occasionally

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