Clinical Trials Assistant & Recruitment Coordinator

Arizona Arthritis and Rheumatology Research, PLLC

Rockville (MD)

On-site

USD 52,000 - 68,000

Full time

12 hours ago
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Job summary

Arizona Arthritis and Rheumatology Research, PLLC is seeking a Clinical Research Coordinator to support patient recruitment, eligibility screening, and enrollment in rheumatology trials. The role involves data entry, regulatory documentation, and close collaboration with physicians and research staff.

The position requires an Associates degree or higher, knowledge of clinical terminology, strong organization, and willingness to travel for Investigator Meetings and site visits.

Qualifications

  • Associates Degree or equivalent.
  • In-depth knowledge of medical procedures and clinical terminology.
  • Strong organizational skills.
  • Ability to develop and maintain professional relationships with providers and research subjects.
  • Maintains confidentiality of patient and study information.
  • Excellent verbal and written communication skills.
  • Ability to lift 20 pounds.
  • Willing and able to travel for Investigator Meetings and other sites.

Responsibilities

  • Assess potential patients' eligibility for inclusion in a protocol.
  • Recruit and enroll patients onto clinical trials according to study protocols.
  • Check eligibility criteria with medical records and staff.
  • Discuss informed consent with patients and document adverse events.
  • Monitor protocol adherence and assist with scheduling visits.
  • Enter data and manage study documentation.
  • Coordinate study supply shipping and inventory as needed.

Skills

Organizational skills
Verbal communication
Written communication
Travel willingness

Education

Associates degree or equivalent
Bachelor's degree in biological sciences or health sciences

Job description

Arizona Arthritis and Rheumatology Research, PLLC is seeking a Clinical Research Coordinator to support patient recruitment, eligibility screening, and enrollment in rheumatology trials. The role involves data entry, regulatory documentation, and close collaboration with physicians and research staff.

The position requires an Associates degree or higher, knowledge of clinical terminology, strong organization, and willingness to travel for Investigator Meetings and site visits.

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