Clinical Research Coordinator I, Strive & Bhs

The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical research and clinical trials related to cardiovascular health and maternal health and diabetes. The Clinical Research Coordinator assists the principal investigators, field coordinator, other clinical research coordinators and study team with study conduct. The Clinical Research Coordinator is able to recruit, follow, and retain study participants, and perform study visits, data collection and entry, and quality control activities according to study protocol independently. Additional responsibilities include recruitment calls and leading health education sessions in a group setting. The Clinical Research Coordinator I is also able to perform procedures required by the study protocol(s), such as blood pressure measurements, anthropometrics, and lab collection. The Clinical Research Coordinator I is responsible for all data and source documentation, adverse event reporting and maintenance of complete regulatory files, under direct supervision.

Required Knowledge, Skills, and Abilities • Must be able to interact well with patients and the general public

• Strong communication skills both verbal and written, report writing, and ability to meet deadlines
• Good team member and experience in working in an office environment

• Ability to acquire and maintain all required CITI training certificates

• Ability to acquire and maintain credentialing at all required institutions

• Willing to travel to conduct clinic visits some days each week

Required Education and/or Experience

• Bachelor’s Degree

Preferred Qualifications • Expressed interest in Clinical Research

• Experience working on a research study or clinic is preferred, but not required

• Experienced with research coordination and teams
• Motivated to learn about Clinical Research and associated regulations

• Competent with technology (MS Office Suite, Excel, PowerPoint; Access; Outlook; SAS; Endnote)