Clinical Research Associate

Clinical Research Associate

• Location:
  
  Los Angeles, California
• Type:
  Contract
• Job #86786

APR Consulting, Inc. has been engaged to identify a Clinical Research Associate

Location: Los Angeles, CA 90025
Position:
Clinical Research Associate
Pay Rate: $29/hr
Duration: 13 weeks
Expected Shift: 40 hrs/week
8am to 5pm

JOB SUMMARY

*** This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and immerse yourself in the energy of our workplace. Please note that hybrid or remote work options are NOT available for this position at this time**
* ** This is not a lab based role*
* Requirements:

• High School Diploma/GED required.

• 1 year Clinical research related experience required.

Preferred:

• Bachelor's degree preferred.

• Chemo, Oncology, or pharmaceutical research experience

• Interested in temp to perm

Primary Duties and Responsibilities:

• Submits research projects (protocols, consent forms, recruitment materials, IRB application, etc.) for human subjects' approval.

• Submits appropriate internal documentation for contract execution. Maintains communication with contracting officers and sponsors of research during the budgeting and negotiating process.

• Develops research project budgets based on protocol requirements and Cedars-Sinai published research costs, ensuring that all anticipated costs are appropriately accommodated and that research protocol, research budget and research subject informed consent documents are consistent.

• Monitors study payments and generates invoices as necessary to ensure adequate funding throughout the course of the trial.

• Ensures timely filing of annual renewals and amendment submissions to IRB.

• Ensures the completion and maintenance of consent forms, case report forms, SAE's and source documents to ensure that research is being conducted according to IRB, FDA, OHRP, HIPAA and other agency guidelines.

• Maintains high quality, up-to-date regulatory files (CITI and other training documents, financial disclosures, FDA forms, CVs, medical licenses, etc.) for research studies.

• Completes appropriate IRB paperwork and submits internal and external Serious Adverse Events (SAEs) and INDSRs to IRB.

• May help coordinate and prepare for institutional, pharmaceutical and internal audits.

• Coordinates site feasibility visits and site initiation visits for potential studies. Completes feasibility questionnaires.

• Provides facility tours to visiting research sponsors, CROs, and other personnel for research-related activities.

• Coordinates and collaborates with internal and external investigators and participating centers in multi-center studies to achieve research goals.

• Participates in weekly research staff meetings.

• Protects rights and research data of research volunteers, including medical records, data, etc. Obtains necessary consent forms, or HIPAA information forms as needed, in research process.

• Performs administrative duties in a timely manner as assigned.

Our client is the one of the largest Healthcare Staffing Provider in the United States, to be assigned at one of their affiliated hospitals/healthcare facilities.

This particular client is requiring that all new hires show proof of vaccination. However, accommodations may be made for those with disabilities or religious reasons who cannot obtain a vaccine.

Since 1980 APR Consulting, Inc. has provided professional recruiting and contingent workforce solutions to a diverse mix of clients, industries, and skill sets nationwide.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Don't miss out on this amazing opportunity! If you feel your experience is a match for this position please apply today and join our team. We look forward to working with you!