Clinical Research Associate I - Beverly Hills, CA
Company: Msccn
Location: Beverly Hills
Posted on: April 3, 2026
|
|
|
Job Description:
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization
works with partner companies to source qualified talent for their
open roles. The following position is available to Veterans,
Transitioning Military, National Guard and Reserve Members,
Military Spouses, Wounded Warriors, and their Caregivers . If you
have the required skill set, education requirements, and
experience, please click the submit button and follow the next
steps. This role follows a hybrid work schedule; however, we can
only consider applicants who will be able to commute to our Los
Angeles work location a few times per week. If hired you must
reside in the commutable area. The Clinical Research Associate I
works under the direction of a Clinical Research Coordinator,
Research Program Administrator, Research Nurse, or other
supervising staff to assist in tasks supporting the
coordination/implementation of noncomplex research studies.
Supports objectives of research studies through noncomplex tasks
such as data collection, prescreening of potential and scheduling
of current research participants, assisting in IRB submission
activities, budget and billing, and ensuring overall compliance
with all federal and local guidelines. Primary Duties and
Responsibilities Works under the direction of a Clinical Research
Coordinator, Research Program Administrator, Research Nurse, or
other supervising staff to assist in tasks supporting the
coordination/implementation of noncomplex research studies.
Collects, evaluates and/or abstracts clinical research data. May
assist in designing forms for data collection/abstraction. Enters
and processes clinical research data into Electronic Data Systems
(EDCs) that are provided by the sponsors. Completes Case Report
Forms (CRFs). Assists with prescreening of potential research
participants for various clinical trials. Schedules research
participants for research visits and research procedures. Provides
supervised patient contact or independent patient contact for long
term follow-up patients only. Assists supervising staff with
regulatory submissions to the Institutional Review Board (IRB)
including submission of Adverse Events, Serious Adverse Events, and
Safety Letters in accordance with local and federal guidelines.
Assists with clinical trial budgets and patient research billing.
Responsible for sample preparation and shipping and maintenance of
study supplies and kits. Ensures compliance with protocol and
overall clinical research objectives. Ensures compliance with all
federal and local agencies including the Food and Drug
Administration (FDA) and local Institutional Review Board.
Maintains research practices using Good Clinical Practice (GCP)
guidelines. Maintains strict patient confidentiality according to
HIPAA regulations and applicable law. May serve as one point of
contact for external sponsors for select trials. May respond to
sponsor inquiries and attend meetings regarding study activity
under the direction of supervising staff. This role follows a
hybrid work schedule; however, we can only consider applicants who
will be able to commute to our Los Angeles work location a few
times per week. If hired you must reside in the commutable area.
Requirements: High School Diploma/GED required. Preferred:
Bachelor's Degree preferred. 1 year Clinical research related
experience preferred. Minimum Salary 24.00 Maximum Salary 32.86
Keywords: Msccn, Vista , Clinical Research Associate I - Beverly Hills, CA, Healthcare , Beverly Hills, California
