Clinical Research Assistant

2 weeks ago


Scottsdale, United States Medix™ Full time

Position Overview:

We are seeking a dedicated and detail-oriented Clinical Research Coordinator Assistant to support the execution of clinical trials. In this role, you will play a vital part in patient recruitment, screening, enrollment, and data coordination, ensuring compliance with study protocols and regulatory requirements.


Key Responsibilities:

  • Patient Recruitment & Enrollment: Identify, recruit, and screen potential study participants in alignment with eligibility criteria.
  • Participant Interaction: Obtain informed consent, schedule study visits, and ensure participants adhere to visit timelines.
  • Assessments & Data Collection: Perform basic assessments, such as vital signs and questionnaires, and document findings accurately.
  • Data Coordination: Maintain and update clinical trial databases, ensuring accuracy and timely entry of participant data.
  • Protocol Compliance: Assist in monitoring study conduct, ensuring all activities are performed according to the protocol, Good Clinical Practice (GCP), and regulatory guidelines.
  • Administrative Support: Coordinate study visit logistics, prepare study materials, and support site audits or monitoring visits as needed.
  • Communication: Act as a liaison between participants, clinical staff, and investigators to address concerns and provide updates.

Qualifications:

  • Bachelor’s degree in a health-related field or equivalent experience in clinical research or patient care.
  • Prior experience in clinical research, patient recruitment, or data entry preferred.
  • Strong interpersonal skills with the ability to engage and build rapport with participants.
  • Excellent organizational skills and attention to detail.
  • Familiarity with clinical trial regulations and GCP is a plus.
  • Proficiency in [Insert tools/software, e.g., EDC systems, Microsoft Office].



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