Clinical Research Coordinator I - All of Us Research Study

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 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.

• Bachelors or Masters degree in Science or closely related field.
• No experience required. One year of research experience preferred.

Preferred:

• 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)  

 

 

• 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.