Clinical Research Coordinator I

About the Role

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.

Key Responsibilities

• 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.

Requirements & Tech Stack

• Collects, maintains, and organizes study information.
• Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office).
• Performs some clinical assessments.
• Proficiency in Microsoft Office Suite.
• Background in clinical research or closely related field.
• Strong communication and organization skills.
• 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).

Qualifications

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