Joule Hiring For Traveling Healthcare Investigator at NA, VT Full Time

Title: Traveling Healthcare Investigator 
Location: Vermont 
Duration: Direct hire
Schedule: Monday through Friday 9-5, 40 hours a week. 3-4 days at one site, then remote, until next travel assignment
Start: ASAP

RESPONSIBLITIES:

• Work closely with the Principal Investigator to oversee the execution of study protocols, delegating study related duties to site staff, as appropriate, and ensuring site compliance with study protocols, study-specific laboratory procedures, standards of Good Clinical
• Practice (GCP), Standard Operating Procedures (SOPs), quality (QA/QC) procedures,
• OSHA guidelines, and other state and local regulations as applicable.
• Read and understand the informed consent form, protocol, and investigator’s brochure
• Be available to see subjects, answer their questions, and resolve medical issues during the study visit
• Sign and ensure that the study documentation for each study visit is completed
• Perform all study responsibilities in compliance with the IRB approved protocol
• Review screening documentation and approves subjects for admission to study
• Review admission documentation and approves subject for randomization
• Provide ongoing assessment of the study subject/patient to identify Adverse Events
• Ensure that serious and unexpected adverse events are reported promptly to the Pl
• Review and evaluates all study data and comments to the clinical significance of any out of range results
• Perform physical examinations as part of screening evaluation and active study conduct
• Provide medical management of adverse events as appropriate

REQUIREMENTS:

• Nurse Practitioner, Physician’s Assistant or Physician with 3+ years of total experience
• Currently licensed in good standing in one or more states
• Minimum of one (1) year of clinical research experience (preferred)
• ·Knowledge of medical and research terminology and procedures and clinical data
• Proficient in GCP, ICH, and Human Research Subjects Protection guidelines, as well as regulatory requirements relating to clinical development and safety compliance with ethical, legal and regulatory standards preferred
• Strength in communication, planning, and time management skills
• Strong People Skills  
• Willingness to travel as needed
• Excellent working knowledge of medical and research terminology
• Excellent working knowledge of federal regulations, good clinical practices (GCP)
• Ability to communicate and work effectively with a diverse team of professionals