Site Research Assistant - Fixed Term

Job Overview
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.

Essential Functions:

• Provide clinical research support to investigators to prepare for and execute assigned research studies.

• 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.
•    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.
• Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.
• Assist research site with coverage planning related to staffing and scheduling for research projects.

Qualifications:

• Bachelor's degree in life sciences or related field.
• Desirable work experience in a clinical environment.
• Working knowledge of Clinical Trials and the principles of Good Clinical Practices (GCP)

• English Level: Intermediate.

• 6 months Fixed Term Contract.

• Locations: CABA, Mar del Plata, Bahia Blanca, Córdoba Capital and Tucuman.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.