Clinical Research Coordinator I - Genetics & Genomic Sciences

Responsibilities

• Obtains informed consent under minimal supervision; provides information regarding the study to participants
• Collections and records study data; regularly speaking with study participants
• Assists in monitoring and interpreting clinical research data for integrity and to prepare reports for study projects, IRB/GCO, study sponsors, etc.
• Performs activities related to clinical research studies, including but not limited to, answering phone calls when on-call, screening patients for eligibility, sending collection kits, attending procedures for collections, processing samples, administering questionnaires
• Secures, delivers and ships clinical specimens under minimal supervision as required by the protocol
• Works closely with the Project Manager to support and develop lab projects with other lab members: Principal Investigator, Researchers, collaborating investigators, volunteers, students, etc.

Qualifications

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