Clinical Research Associate II

Cedars-Sinai; Los Angeles (CA); On-site; USD 60,000 - 90,000; Full time

Job summary

Cedars-Sinai is seeking a Clinical Research Associate II to work closely with coordinators and nurses to coordinate and implement increasingly complex research studies. The role involves data collection, prescreening, scheduling, and supporting IRB submissions, budgeting, and regulatory compliance under GCP and HIPAA guidelines.

The CRA II will serve as an independent contact with sponsors, IRB, and participants, providing training to junior staff and coordinating ad hoc study activities.

Qualifications

• High School Diploma or GED is required.
• Minimum of 1 year of clinical research-related experience preferred.
• Bachelor's Degree in Science, Sociology, or related field preferred; CRC certification is a plus.

Responsibilities

• Coordinate and implement increasingly complex clinical research studies.
• Assist in IRB submission activities and regulatory coordination.
• Manage data collection, screening, scheduling, and CRF completion.
• Support budgeting, patient billing, and adherence to GCP/HIPAA.

Education

High School Diploma or GED

Bachelor's Degree in Science, Sociology, or related field

Clinical Research Certification (SOCRA/ACRP)

Tools

Electronic Data Systems (EDCs)

Job description

Job Description

The Clinical Research Associate II works independently but in close collaboration with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, other supervising staff to coordinate and/or implement increasingly complex 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. Provides increasingly complex and independent support for studies by serving as the independent contact with sponsors, IRB, and research participants, providing training, education to junior level staff, and coordination of ad hoc activities related to studies. May serve independently as study coordinator for minimal number of noncomplex research studies or projects.

Responsibilities

• Works independently under minimal direction from a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to coordinate and/or implement increasingly complex 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).
• Independently prescreens potential research participants for various clinical trials. Schedules research participants for research visits and research procedures. May provide increasingly independent contact with research participants and/or conduct research participant visits independently.
• Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB). May work directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, Safety Letters, etc in accordance with local and federal guidelines.
• Assists with clinical trial budgets and patient 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 the primary point of contact for external sponsors for select trials. Responds to sponsor inquiries and attends meetings regarding study activities.
• Participates in and provides training and education to other Clinical Research Associates. May assist in coordinating activities of other associates to ensure compliance with protocol and clinical research objectives.
• Participates in centralized activities such as auditing, Standard Operating Procedure development, etc.
• May participate in the development of Investigator Initiated trials for Investigational New Drug applications and/or Device applications
• May provide coordination of minimal number of noncomplex research studies or projects independently. May provide coverage for study coordination activities of supervising staff when needed to ensure minimal disruption to study objectives.

Qualifications

Required Qualifications

• High School Diploma or GED.
• Minimum of 1 year of clinical research-related experience.

Preferred Qualifications

• Bachelor's Degree in Science, Sociology, or a related field.
• Clinical Research Certification, such as SOCRA or ACRP certification.