Clinical Research Coordinator - ICONMA, LLC
South San Francisco, CA
About the Job
Clinical Research Coordinator
Location: South San Francisco, CA/Hybrid
Duration: 6 Months
Description:
Project Overview:
This role will support digital/wearable medical device clinical research studies conducted by Clinical Development that take place at the Verily Clinical Research Site in South San Francisco.
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.
Responsibilities will encompass advanced support for critical programs within the product management functions.
You will have a leadership role in program planning and execution, playing a key part in strategy development and implementation.
Collaborating with HR Business Partners, managers, employees, and central People Operations colleagues will be central to your role.
Responsibilities will include overseeing program activities, ensuring impeccable documentation, and taking the initiative to address complex challenges while supporting the team's success.
This level demands a high level of expertise in program management, exceptional organizational skills, and the ability to guide and mentor junior coordinators within the department.
As an equal opportunity employer, ICONMA pride itself on creating an employment environment that supports and encourages the abilities of all persons regardless of race, colour, gender, age, Sexual orientation, citizenship, or disability.
Location: South San Francisco, CA/Hybrid
Duration: 6 Months
Description:
Project Overview:
This role will support digital/wearable medical device clinical research studies conducted by Clinical Development that take place at the Verily Clinical Research Site in South San Francisco.
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.
Responsibilities will encompass advanced support for critical programs within the product management functions.
You will have a leadership role in program planning and execution, playing a key part in strategy development and implementation.
Collaborating with HR Business Partners, managers, employees, and central People Operations colleagues will be central to your role.
Responsibilities will include overseeing program activities, ensuring impeccable documentation, and taking the initiative to address complex challenges while supporting the team's success.
This level demands a high level of expertise in program management, exceptional organizational skills, and the ability to guide and mentor junior coordinators within the department.
As an equal opportunity employer, ICONMA pride itself on creating an employment environment that supports and encourages the abilities of all persons regardless of race, colour, gender, age, Sexual orientation, citizenship, or disability.
Source : ICONMA, LLC