Edc/Clinical Devices Research Coordinator

Description:

Overall Responsibilities:

• The Clinical Research Coordinator, under the oversight of the Clinical Trial Manager and PI, is responsible for independently conducting clinical research sessions with study participants.
• These sessions will be conducted on-site in South San Francisco and virtually.

Top 3 Daily Responsibilities:

• Conduct Clinical Research Coordinator activities for assigned clinical research device studies including consenting participants, conducting study sessions, maintaining device accountability, and completing data entry into the Electronic Data Capture (EDC) system.
• Maintain Investigator Site Files and support Sponsor eTMF Maintenance.
• Coordinate study participant recruitment efforts and ensure participants are compensated for their study participation.

Mandatory:

Education:

• BS/BA degree in life science, health science, RN, or related field.
• 3-5 years of professional working experience as a Clinical Research Coordinator.
• Working knowledge of GCP and FDA Regulations.
• Proficiency in MS Word, Excel PowerPoint, or Suite.
• Experience utilizing Electronic Data Capture (EDC) systems for clinical studies.

Desired:

• Desired Experience with digital medical device research studies.
• Experience maintaining an Electronic Trial Master File (eTMF).

Education:

• BS/BA degree in life science, health science, RN, or related field.