Quelle:
Für dieses Angebot liegt keine vollständige Übersetzung in der gewählten Sprache vor. Unten sehen Sie den Originalinhalt.
Research Study Coordinator, Research Clinical Trials, Full Time, Day
Valleyhealth
Vereinigte Staaten
; Vereinigte Staaten (whole country)
29.34-36.67 USDper hour
Publication date: 12/11/2026
Coordinates and administers research study associated activities under the direction of the Principal Investigator (PI) and Research Nurse Manager/Supervisor. Assists in project planning; coordinates and implements clinical research; acts as the patient advocate by assuring the safety, consistency, and accuracy of the treatment regimen as dictated by the PI and the protocol, and coordinates all activities specifically related to the implementation of the treatment regimen, including consenting subjects when appropriate, scheduling appointments and ancillary services, registering patients for billing compliance and data collection. Remains current in all regulatory education, training and certification requirements.
Responsibilities
Coordinates and administers research study associated activities under the direction of the Principal Investigator (PI) and Research Nurse Manager/Supervisor; Assists in project planning; Coordinates and implements clinical research; Acts as the patient advocate by assuring the safety, consistency, and accuracy of the treatment regimen as dictated by the PI and the protocol; Coordinates activities related to the implementation of the treatment regimen, including consenting subjects when appropriate; Schedules appointments and ancillary services; Registers patients for billing compliance and data collection; Remains current in all regulatory education, training and certification requirementsRequirements
Bachelor's degree or minimum ten years' experience as a study coordinator; Medical terminology; Utilizes computer programs, software, Excel, web-based databases and data entry; Effective oral and written communication skills; Ability to perform work accurately and pay attention to details; Ability to function competently in stressful situations and changing work environments; Ability to work cooperatively within a multidisciplinary team; Effective time management skillsNice to have
CPR certification; Phlebotomy certification; IATA certification; CCRP or CCRC certification; CITI certification; Knowledge of ICH-GCPBenefits
Medical/Prescription, Dental & Vision Discount Program (Full Time/Part Time Employees); Group Term Life Insurance and AD&D (Full Time Employees); Flexible Spending Accounts and Commuter Benefit Plans; Supplemental Voluntary Benefits (e.g. Short-term and Long-term Disability, Whole Life Insurance, Legal Support, etc.); 6 Paid Holidays, Paid Time Off (varies), Wellness Time Off, Extended Illness; Retirement Plan; Tuition Assistance; Employee Assistance Program (EAP); Valley Health LifeStyles Fitness Center Membership Discount; Day Care Discounts for Various Daycare FacilitiesHow to apply
Apply online: https://www.jobs.pl/en/oferta/102585163/aplikuj
JOBS.pl · https://www.jobs.pl/de/research-study-coordinator-research-clinical-trials-full-time-day-oferta-102585163






