Clinical Research Coordinator I - All of Us Research Study (Bi-Lingual Spanish Preferred)

HealthcareClinical Researcher
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Quick Summary

Requirements Summary

answering phone calls, screening participants for eligibility, scheduling/coordinating study visits, administering lifestyle questionnaires. Assist in IRB/GCO applications as needed.

Technical Tools
HealthcareClinical Researcher

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office).

The Clinical Research Coordinator I will participate in clinical research activities related to the All of Us study, a NIH initiative to enroll one million people across the U.S. to help build one of the most diverse health databases in history. The Clinical Research Coordinator I will be responsible for obtaining informed consent, collecting and processing biospecimens, performing some clinical assessments, and collecting, maintaining, and organizing study information. They will also assist in preparing documents (for e.g., Institutional Review Board, Grants and Contracts Office) and performing other study related activities as needed.  

  • Obtain informed consent and educate participants regarding study requirements.
  • Collect and record study data and input all information into a database.  
  • Collect, process, deliver and ship clinical specimens as required by the protocol.  
  • Assist in activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, scheduling/coordinating study visits, administering lifestyle questionnaires.
  • Assist in IRB/GCO applications as needed.  
  • Maintain source documents and subject files in accordance with hospital procedures. Ensure accurate and complete compilation of subject data through chart reviews.  
  • Perform other related duties as requested.
  • Bachelors or Masters degree in Science or closely related field.
  • No experience required. One year of research experience preferred.

Nice to Have

~1 min read
  • Proficiency in Microsoft Office Suite  
  • Background in clinical research or closely related field
  • Strong communication and organization skills
  • Passion for patient care and clinical research  
  • Demonstrated ability to work effectively, communicate clearly, and accomplish goals  
  • Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment  
  • Effective interpersonal skills, able to establish good working relationships and collaborate with networks of employees at all levels, able to foster cooperation in others
  • Bilingual in Spanish (preferred but not required)  

 

 

 

Location & Eligibility

Where is the job
United States
On-site within the country
Who can apply
US

About this job

Who can apply
United States
Posted
22 days ago
Employer
has 2,584 open jobs on Jobera.

Listing Details

Posted
September 22, 2026
First seen
September 26, 2026
Last seen
October 6, 2026

Posting Health

Days active
17
Repost count
0
Trust Level
19%
Scored at
October 14, 2026

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Clinical Research Coordinator I - All of Us Research Study (Bi-Lingual Spanish Preferred)