Travel Clinical Research Coordinator - $1,665 per week

Integrated Healthcare Services

  • Rochester, MN
  • 5 days ago
  • $1,665 Per Week

Highlights

Responsibilities may include participant scheduling, responding to patient communications, supporting blood draw scheduling, kit management, research documentation, and other study coordination activities. Associate's degree/college diploma/certificate program with at least one (1) year of experience, or Associate's in Clinical Research from an accredited academic institution without experience.

Numbers & Facts

LocationRochester, MN

Description

Integrated Healthcare Services is seeking a travel Clinical Research Coordinator for a travel job in Rochester, Minnesota.

Job Description & Requirements

  • Specialty: Clinical Research Coordinator
  • Discipline: Allied Health Professional
  • Duration: 51 weeks
  • 40 hours per week
  • Shift: 8 hours, days
  • Employment Type: Travel

Schedule Notes
Mon-Fri, 40 hours per week
Flexible start/end times between approximately 7:00 AM and 5:00 PM, on site in Rochester, MN, Mayo Clinic Harwick Building
No holidays, No Call.

Job Title: Assoc. Clinical Research Coord Rochester

Location: Rochester

Job Summary:
Receives direction from principal investigator, supervisor, or other staff involved in research protocol(s). Interacts with various departments within the institution. Works cooperatively with other investigators and personnel at all levels. Interacts with research participants, other research centers, and sponsoring companies to resolve problems and ensure efficient completion of research studies.

Required Qualifications:

  • High school diploma with at least three (3) years of experience.
  • Associate's degree/college diploma/certificate program with at least one (1) year of experience, or Associate's in Clinical Research from an accredited academic institution without experience.
  • Bachelor's degree with experience in a clinical setting or related field.


Preferred Qualifications:

  • One (1) year of clinical research experience.
  • Medical terminology course.
  • Experience coordinating patient-facing activities, scheduling, documentation, and working within regulated environments.
  • Strong attention to detail.
  • Experience with service excellence and repetitive tasks.


Additional Information:

  • Responsibilities may include participant scheduling, responding to patient communications, supporting blood draw scheduling, kit management, research documentation, and other study coordination activities.
  • Some travel may be required.

Integrated Healthcare Services Job ID #37734720. Pay package is based on 8 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Assoc. Clinical Research Coord Rochester

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