Clinical Research Coordinator (Cordoba)

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, 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.
• Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.
• Provide training to new investigator site staff members on study-specific topics and requirements.  Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.
• 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 Availability to work 16h per week, fixed term contract. • 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 • Working knowledge of clinical trials • Working knowledge of the principles of Good Clinical Practices (GCP) • In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules • Skill in carrying out required clinical procedures such as intravenous catheter insertion and spirometry testing • Good skill in using MS Windows and Office applications such as Access, Outlook and Word • Excellent interpersonal skills • Ability to pay close attention to detail • Ability to establish and maintain effective working relationships with coworkers, managers and clients •  Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies