**Home based - All Europe**

" 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."

PURPOSE

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
• Fluent in Polish
• Ability to speak additional European language