Cedars-Sinai Clinical Research Associate I - Per Diem - All of Us Program in Los Angeles, California
The California Precision Medicine Consortium (CaPMC) is part of the national All of Us Precision Medicine Research Program which aims to enroll 1 million participants living in the U.S. to contribute their health data for research. This national study will provide researchers and scientists access to biospecimens, genetic data, medical records, and person-generated health data to advance precision medicine in the U.S. CaPMC includes UC Davis, UC San Diego, UC Irvine, UC San Francisco, USC, and Cedars Sinai. Clinical Research Associates for this research program will work with the research team to review communication materials and implement social media strategies to advance public understanding of precision medicine and the All of Us research program.
The Clinical Research Associate I - Per Diem will work directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. This role evaluates and abstracts research data and ensures compliance with protocol and research objectives. Position is responsible for completing case report forms (CRFs), entering clinical research data, and assist with regulatory submissions to the IRB. This role will comply with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care.
In addition the CRA I - Per Diem will be responsible for the following:
Work primarily with the engagement lead, project lead, and study coordinators to assist the engagement team for the program.
May work remotely, on campus, and occasionally be asked to work off-site at events (under the supervision of study lead and/or study coordinators).
Attend weekly check-ins and team meetings.
Assist team with planning and implementation of social media strategies.
Interact with participants by answering and returning telephone calls.
Answer participant questions and provide information regarding the study, explaining procedures, and consent process.
Interact with online users and triage online comments to appropriate personnel.
Report issues or concerns to engagement/study leads as they arise and maintain good communication with team.
Assist with other engagement and recruitment activities, as appropriate, to promote visibility and awareness for the program.
May be responsible for the pick-up and delivery of clinical research-related items such as bio-specimens.
BA/BS degree, required
Understanding of general research objectives.
Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.