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Weekend Historical Researcher Jobs in Arizona (NOW HIRING)

Swift Logistics

Weekend Account Manager

Phoenix, AZ

$24.47 - $34.95/hr

Swift Transportation has been an Industry leader for many years with a profound history dating back ... Research and code all applicable service failures. * Maintain current reporting, contact ...

Swift Logistics

Weekend Account Manager

Phoenix, AZ · On-site

$24.47 - $34.95/hr

Swift Transportation has been an Industry leader for many years with a profound history dating back ... Research and code all applicable service failures. * Maintain current reporting, contact ...

Swift Logistics

Weekend Account Manager

Phoenix, AZ · On-site

Swift Transportation has been an Industry leader for many years with a profound history dating back ... Research and code all applicable service failures. * Maintain current reporting, contact ...

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Clinical research Coordinator

Liver Institute PLLC

Tucson, AZ • On-site

$17 - $20/hr

Part-time

Posted 9 days ago

Job description

About the Role:
Liver Institute PLLC in Tucson, AZ is looking for a dedicated Clinical Research Coordinator (CRC) to join our specialized team. This is an exciting opportunity to contribute to meaningful clinical research in a focused, patient-centered hepatology practice. If you're passionate about advancing medical science and making a real difference in patients' lives, we want to hear from you!

Qualifications
Bachelor's degree or Higher Required
Minimum of one year of experience as a clinical research coordinator or two years of healthcare experience with patient interaction or related experience
  • Excellent interpersonal and relationship-building skills with the ability to communicate effectively with sponsors, research participants, physicians, and clinic staff.
  • Strong organizational, time management, and multitasking abilities with exceptional attention to detail.
  • Experience with patient recruitment, outreach, or sales/customer engagement is highly preferred.
  • Willingness to work a flexible schedule as needed, including occasional early mornings, evenings, or weekends to accommodate participant visits.
  • Spanish-speaking (bilingual English/Spanish) preferred.
  • Healthcare experience, including phlebotomy skills, is preferred; candidates willing to obtain phlebotomy training will also be considered.
  • Educational background in biology, health sciences, nursing, public health, or another life science discipline preferred.
  • Strong problem-solving skills with the ability to adapt in a changing environment.
  • Demonstrates professionalism, compassion, and a patient-centered approach while maintaining confidentiality and regulatory compliance.
Responsibilities
  • Coordinated clinical research studies with multidisciplinary teams.
  • Screened, educated, and enrolled study participants.
  • Conducted informed consent with participants and caregivers.
  • Monitored participant safety and reported adverse events.
  • Documented study activities in compliance with regulatory requirements.
  • Reviewed and resolved data queries daily.
  • Maintained regulatory and study documentation.
  • Collected medical history and concomitant medications.
  • Requested and reviewed hospital medical records.
  • Assisted investigators with clinical trial procedures.
  • Processed, prepared, and shipped biological specimens.
  • Prepared laboratory requisitions for protocol-required testing.
  • Conducted protocol-specific participant interviews and assessments.
  • Participated in quality assurance audits.
  • Ensured compliance with GCP, protocol, and sponsor requirements.
  • Performed additional duties as assigned by the Principal Investigator.
The job is onsite, and no relocation assistance is provided for this position.