Research Coordinator Jobs

About The Position

Requirements

• Ability to perform independently or with general direction at the fully operational journey level.
• Proficiency in coordinating data collection and study operations.
• Experience with electrophysiological sleep equipment and electroencephalography collection.
• Skills in managing and reporting study results.
• Experience in creating, cleaning, updating, and managing databases and comprehensive datasets and reports.
• Ability to coordinate staff work schedules and assist with training.
• Experience managing protocols in online systems (e.g., Committee on Human Research, Western Institution Board).
• Experience with protocol renewals and modifications.
• Ability to participate in protocol review and writing for IRB approval.
• Knowledge of compliance with relevant regulatory agencies.
• Skills in overseeing study data integrity and implementing quality control procedures.
• Ability to interface with departments for approvals.
• Proficiency in maintaining regulatory documents.
• Ability to prepare at-home movement and sleep measuring devices.
• Experience administering and analyzing sleep and circadian recordings.
• Experience administering cognitive tests.
• Reliable transportation to various locations throughout the Bay Area.
• Flexible evening hours.
• Flexible daytime hours.

Responsibilities

• Execute, manage, and coordinate research protocols.
• Coordinate data collection and operations of concurrent clinical research studies.
• Coordinate activities in research studies focused on sleep disruption in healthy aging and neurodegenerative diseases.
• Act as intermediary between services and departments.
• Oversee data and specimen management.
• Utilize electrophysiological sleep equipment and electroencephalography collection.
• Manage and report on study results.
• Create, clean, update, and manage databases and comprehensive datasets and reports.
• Coordinate staff work schedules and assist with training of Assistant CRCs.
• Manage Investigator’s protocols in the Committee on Human Research and Western Institution Board online systems, including renewals and modifications.
• Participate in the review and writing of protocols to ensure institutional review board approval.
• Help assure compliance with all relevant regulatory agencies.
• Oversee study data integrity.
• Implement and maintain periodic quality control procedures.
• Interface with departments to obtain UCSF approval prior to study initiation.
• Maintain all regulatory documents.
• Report study progress to investigators and attend team meetings.
• Prepare at-home movement and sleep measuring devices.
• Administer and analyze sleep and circadian recording.
• Administer cognitive tests.
• Perform other duties as assigned.

Benefits

• Total compensation information available at https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html