Clinical Research Coordinator I - All of Us Research Program

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.

Qualifications

• Bachelor's or Master's degree in Science or closely related field.
• No experience required. One year of research experience preferred.

Preferred Qualifications

• Proficiency in Microsoft Office Suite.
• 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).