IQVIA
Clinical Trial Nurse - Gilbert, AZ
Job Overview:
Part‑time – 8 hours per month onsite support. Coordinate and participate in clinical research studies, ensuring that all studies are conducted in accordance with protocol, sponsor SOPs, good clinical practice (GCP), and applicable local regulations.
Responsibilities
Provide clinical research support to investigators for study preparation and execution.
Review study protocols, source document forms, other study‑specific documents, and electronic data capture systems.
Collect and submit regulatory and ethics documentation (FDA and other regulatory bodies).
Recruit and screen patients, maintain subject screening and enrollment logs.
Orient research subjects to the study purpose, procedures, and protocol.
Maintain source documentation per protocol, adhering to GCP/ICH principles.
Schedule and execute study visits; perform study procedures under PI supervision.
Handle specimen collection, lab logistics, and prepare specimen tubes.
Monitor subject safety, report adverse events to the PI, study team, and IRBs.
Correspond with research subjects to troubleshoot study‑related questions.
Participate in routine meetings with site staff and investigators to confirm task assignments.
Perform data quality checks and resolve queries.
Conduct complex procedures such as ECG, lab sample collection, spirometry, vital signs, dose verification, cardiac telemetry, and questionnaire administration.
Update and maintain site staff skills, training, and current best nursing practices.
Assist investigators in safeguarding subject well‑being and maintaining required standards.
Requirements
Maintain adherence to investigator site staff training requirements, auditing, and training records.
Provide guidance and supervision to lower‑level site staff.
Participate in study process reviews and enhancement efforts to support site budget control and facility development.
Prepare for study monitoring visits, audits, and regulatory inspections.
Adhere to SOPs and other directives throughout all processes.
Assist research sites with coverage planning, staffing, and scheduling for research projects.
Compensation Hourly base rate: $50.00–$60.00 (actual pay may vary based on qualifications, location, and schedule). Additional benefits may include incentive plans, bonuses, health and welfare benefits.
Equal Opportunity IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, veteran status, or any other status protected by applicable law.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence, accelerating the development and commercialization of innovative medical treatments worldwide.
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Part‑time – 8 hours per month onsite support. Coordinate and participate in clinical research studies, ensuring that all studies are conducted in accordance with protocol, sponsor SOPs, good clinical practice (GCP), and applicable local regulations.
Responsibilities
Provide clinical research support to investigators for study preparation and execution.
Review study protocols, source document forms, other study‑specific documents, and electronic data capture systems.
Collect and submit regulatory and ethics documentation (FDA and other regulatory bodies).
Recruit and screen patients, maintain subject screening and enrollment logs.
Orient research subjects to the study purpose, procedures, and protocol.
Maintain source documentation per protocol, adhering to GCP/ICH principles.
Schedule and execute study visits; perform study procedures under PI supervision.
Handle specimen collection, lab logistics, and prepare specimen tubes.
Monitor subject safety, report adverse events to the PI, study team, and IRBs.
Correspond with research subjects to troubleshoot study‑related questions.
Participate in routine meetings with site staff and investigators to confirm task assignments.
Perform data quality checks and resolve queries.
Conduct complex procedures such as ECG, lab sample collection, spirometry, vital signs, dose verification, cardiac telemetry, and questionnaire administration.
Update and maintain site staff skills, training, and current best nursing practices.
Assist investigators in safeguarding subject well‑being and maintaining required standards.
Requirements
Maintain adherence to investigator site staff training requirements, auditing, and training records.
Provide guidance and supervision to lower‑level site staff.
Participate in study process reviews and enhancement efforts to support site budget control and facility development.
Prepare for study monitoring visits, audits, and regulatory inspections.
Adhere to SOPs and other directives throughout all processes.
Assist research sites with coverage planning, staffing, and scheduling for research projects.
Compensation Hourly base rate: $50.00–$60.00 (actual pay may vary based on qualifications, location, and schedule). Additional benefits may include incentive plans, bonuses, health and welfare benefits.
Equal Opportunity IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, veteran status, or any other status protected by applicable law.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence, accelerating the development and commercialization of innovative medical treatments worldwide.
#J-18808-Ljbffr