Full-Time

Sub Investigator

Nurse Practitioner

Confirmed live in the last 24 hours

Professional Case Management

Professional Case Management

Compensation Overview

$97.2k - $153.4kAnnually

Mid

Oklahoma City, OK, USA

Category
Nursing & Allied Health Professionals
Medical, Clinical & Veterinary
Required Skills
Word/Pages/Docs
Google Cloud Platform
Excel/Numbers/Sheets
Requirements
  • Advanced practice degree NP
  • Two(2) year of experience as an Advanced Practitioner
  • Two (2) year of experience starting and performing phlebotomy, IVs, subcutaneous injections, collecting vital signs, ECG, and urine collection
  • One (1) year of recent clinical research experience preferred
  • Excellent computer Skills, including Microsoft Outlook, Word, Excel, and PowerPoint
  • Current unrestricted licensure to practice as an Advanced Practitioner (NP or PA) in the state to which the candidate is assigned
  • Current BLS certification required
  • CITI, GCP, and IATA preferred
Responsibilities
  • Serves as a leader to the study team to execute clinical trials by mentoring and training staff in the conduct of clinical trials, protocol requirements, communication, and trial management skills
  • Screens and confirms subject eligibility in assigned clinical trials in accordance with the Health Insurance Portability and Accountability Act (HIPAA) standards
  • Performs pediatric, adult, and geriatric participant visits, including but not limited to medical history collection, medication reconciliation, physical exam, and health education
  • Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and SOPs
  • Implement and coordinate assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports
  • As delegated, administers medications, investigational products, and vaccinations
  • As delegated, assess serious and adverse events as related to investigational product
  • Incorporate understanding of product development lifecycle and significance of protocol design including critical data points when planning for each assigned protocol
  • Perform clinical duties (e.g., Drug preparation and administration, phlebotomy, ECG, lab processing) within scope
  • Assists in coordinating research subject's consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met
  • Assist with electronic data entry
  • Reviews new protocols and other materials provided by study sponsors and gives input to the Principal Investigators (PIs), site leadership, and virtual Clinical Research Coordinators, as applicable, regarding nursing and research issues in order to resolve financial and clinical feasibility
  • Helps ensure that all study related activities are complete including returning supplies, returning unused stock of study drug/devices, and confirming that all queries are complete
  • Maintains current knowledge of departmental functions through reading literature, attending workshops, seminars, and conferences, and by participating in professional organizations
  • Assists in conducting audits of research studies to check the accuracy, integrity, and consistency of the research studies
  • Works collaboratively with physicians, nurses, clinical research specialists, leaders, family members, key care givers and any ancillary medical personnel as appropriate
  • Follows ALCOA +C good documentation practices. Maintains compliance with OSHA, HIPPA and State Board of Nursing
  • Supports Community Engagement team with building the community and developing relationships within that community to assist with the recruitment of participants, such as attending community events, speaking with physicians / healthcare professionals and people across diverse cultures and backgrounds
  • Evaluate potential subjects for participation in clinical trials including phone and in person prescreens
  • Create and execute recruitment strategies in conjunction with patient recruitment staff
  • Performs other duties as assigned including but limited to home visits, recruitment, and community engagement activities, which may occur after hours and/or on weekends
  • Regular and reliable attendance with the ability to work after hours/weekends as needed as well as rotating on-call shifts that may include weeknights, weekends, and holidays
  • Any other duties needed to help drive to our vision, fulfill our mission, and abide by EmVenio’s values
Professional Case Management

Professional Case Management

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