Pediatric Diabetes Clinical Research Associate I - Onsite

Children's Minnesota; Saint Paul (MN); Vor Ort; USD 65.000 - 90.000; Vollzeit

Zusammenfassung

Children’s Minnesota in St Paul, MN is seeking a Clinical Research Associate I to support our research team in conducting departmental projects. The role involves study startup, data coordination, regulatory submissions, and close collaboration with families to obtain informed consent and coordinate visits.

The ideal candidate holds a baccalaureate degree (or 4 years of related clinical research experience) and demonstrates strong attention to detail, communication, and multitasking

Qualifikationen

• High attention to detail with strong written and oral communication skills.
• Strong computer skills beyond basic familiarity with common hardware and software systems.
• Ability to assist staff working on multiple projects.
• Experience working with pediatric populations (preferred).

Aufgaben

• Perform study startup, implementation, and closeout activities
• Assist research team with coordination and entry of research data
• Assist with regulatory submissions to the Institutional Review Board, and maintain compliance with all federal and local agencies in accordance with Good Clinical Practice guidelines
• Interact with patients and families for securing informed consent, scheduling research visits, and collection of data
• Maintain documentation for regulatory binder, adverse event reporting, and communications between sponsors and sites
• Other special skills specific to assigned research area may include phlebotomy, sample collection, processing or shipping, ECGs, chart abstraction or other duties as assigned
• Manage personal career development and administrative tasks

Kenntnisse

Attention to detail

Written & spoken communication

Computer skills

Multitasking

Pediatric experience

Ausbildung

Baccalaureate degree or 4 years relevant clinical research

Jobbeschreibung

Children’s Minnesota in St Paul, MN is seeking a Clinical Research Associate I to support our research team in conducting departmental projects. The role involves study startup, data coordination, regulatory submissions, and close collaboration with families to obtain informed consent and coordinate visits.

The ideal candidate holds a baccalaureate degree (or 4 years of related clinical research experience) and demonstrates strong attention to detail, communication, and multitasking