RN Clinical Research Coordinator: Impactful Trials

AdventHealth

Winter Park (FL)

Presencial

USD 66 000 - 110 000

Tempo integral

Há 8 dias

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

Ultrapassa os filtros ATS

Vantagens oferecidas por esta oferta de emprego

Medical insurance
Dental insurance
Vision insurance
Life insurance
Disability insurance
403-B retirement plan
Parental leave
Career development resources
Mental health resources
Pet benefits

Resumo da oferta

AdventHealth in Winter Park, FL seeks a Registered Nurse to coordinate informed consent and participant eligibility for clinical trials. You will serve as the primary contact for researchers, participants and hospital departments, ensuring accurate documentation and adherence to study protocols.

The role requires RN licensure, strong clinical skills, and the ability to manage multiple tasks in a fast-paced research environment.

Qualificações

  • Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures within scope of practice.
  • Work independently in a fast-paced clinical or research environment.
  • Knowledge of HIPAA data protection and patient advocacy.
  • Strong communication with participants, investigators and staff.
  • Experience with data entry and documentation in clinical research settings.

Responsabilidades

  • Execute and coordinate the informed consent process for participants in clinical trials.
  • Screen potential participants for eligibility.
  • Provide detailed information about studies to potential participants.
  • Maintain accurate records of consent and related discussions.
  • Coordinate biospecimen collection and HIPAA-protected data linkage.

Conhecimentos

Clinical tasks
HIPAA awareness
Communication
Independent worker
Microsoft Office

Formação académica

Associate's Nursing (Required)
Bachelor's Nursing (Preferred)

Ferramentas

Microsoft Office

Descrição da oferta de emprego

AdventHealth in Winter Park, FL seeks a Registered Nurse to coordinate informed consent and participant eligibility for clinical trials. You will serve as the primary contact for researchers, participants and hospital departments, ensuring accurate documentation and adherence to study protocols.

The role requires RN licensure, strong clinical skills, and the ability to manage multiple tasks in a fast-paced research environment.

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