6 дней назад
Nurse Practitioner or Physician Assistant (Sub Investigator) - Part-time
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Nurse Practitioner or Physician Assistant (Sub Investigator) - Part-time (Clinical Research): Conducting study visits, screening participants, collecting patient data, and maintaining clinical trial documentation with an accent on protocol compliance, participant safety, and regulatory standards. Focus on reviewing clinical results, entering accurate data, and collaborating with Principal Investigators and interdisciplinary research teams.
Location: Onsite at 755 Mt Vernon Highway NE, Suite 250, Atlanta, GA 30328, USA
Company
Wake Research operates a network of clinical research sites supporting biopharmaceutical, biotechnology, medical device, pharmaceutical, and clinical research organizations.
What you will do
- Review and follow assigned clinical study protocols.
- Support participant screening and eligibility assessment with the Principal Investigator or Medical Director.
- Conduct study visits and perform protocol-required procedures.
- Maintain case report forms, patient charts, and study documentation.
- Review laboratory results, imaging reports, and other study-specific data.
- Collect and enter clinical trial data while protecting participant safety and confidentiality.
Requirements
- Master’s degree.
- Active Nurse Practitioner or Physician Assistant license.
- Current Advanced Cardiovascular Life Support (ACLS) certification.
- Phlebotomy training.
- Knowledge of FDA regulations, ICH Good Clinical Practice (GCP), and applicable ISO standards.
- Strong communication, organizational, problem-solving, computer, and teamwork skills.
Nice to have
- At least two years of clinical research or sub-investigator experience.
- IV and infusion experience.
Culture & Benefits
- Part-time contract schedule of approximately 20–25 hours per week.
- 1099 contract arrangement.
- Work in a clinical research environment focused on regulatory compliance, data quality, and participant safety.
- Opportunity to support studies as a Study Coordinator in a limited capacity.
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