
Job Overview
Employment Type
Full-time
Compensation
Hourly
Range $24.00 - $34.64
Work Schedule
Standard Hours
Benefits
Health Insurance
Dental Insurance
Paid Time Off
Retirement Plan
Professional development opportunities
Employee wellness programs
competitive salary
Job Description
Cedars-Sinai is a world-renowned healthcare organization and research institute dedicated to providing exceptional patient care, pioneering medical research, and innovative treatments. Within this reputable establishment, The Angeles Clinic & Research Institute has earned an international reputation as a leader in cancer research and treatment. The Clinic specializes in developing new cancer therapies and combines experimental and traditional treatment approaches to offer patients the best possible outcomes. Their team comprises board-certified, fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists who collaborate closely to advance cancer care and innovate therapeutic options for patients worldwide. Cedars-Sinai emphasizes inclusivity and diversity, reflecting the culturally and ethnically varied community it serves. The organization prides itself on fostering a multifaceted environment that promotes creativity, scientific advancement, and the highest standard of care.
The Research Associate II position at Cedars-Sinai plays a pivotal role in the successful administration and management of critical regulatory documents essential for clinical research studies. This role requires a high level of expertise and dedication to ensure research protocols, consent forms, recruitment materials, and IRB applications are timely, complete, accurate, and compliant with regulatory standards. The Research Associate II coordinates contract negotiations, develops research project budgets, monitors study payments, and tracks amendments and renewals to maintain operational efficiency and regulatory adherence. Additionally, the position involves maintaining up-to-date regulatory files, ensuring compliance with guidelines from IRB, FDA, OHRP, HIPAA, and other agencies. The role also supports audits, feasibility assessments, and collaborations with internal and external investigators to facilitate multi-center research initiatives.
This position is a key contributor to the smooth operation and regulatory compliance of cancer research protocols at Cedars-Sinai, supporting the organization’s mission to push boundaries in clinical oncology research and provide cutting-edge treatment options to patients. Research Associates at Cedars-Sinai benefit from working in a supportive, innovative, and multidisciplinary environment that prioritizes employee growth and patient outcomes equally. This role is ideal for motivated individuals seeking to advance their career in clinical research while making a meaningful contribution to groundbreaking medical discoveries and patient care excellence.
The Research Associate II position at Cedars-Sinai plays a pivotal role in the successful administration and management of critical regulatory documents essential for clinical research studies. This role requires a high level of expertise and dedication to ensure research protocols, consent forms, recruitment materials, and IRB applications are timely, complete, accurate, and compliant with regulatory standards. The Research Associate II coordinates contract negotiations, develops research project budgets, monitors study payments, and tracks amendments and renewals to maintain operational efficiency and regulatory adherence. Additionally, the position involves maintaining up-to-date regulatory files, ensuring compliance with guidelines from IRB, FDA, OHRP, HIPAA, and other agencies. The role also supports audits, feasibility assessments, and collaborations with internal and external investigators to facilitate multi-center research initiatives.
This position is a key contributor to the smooth operation and regulatory compliance of cancer research protocols at Cedars-Sinai, supporting the organization’s mission to push boundaries in clinical oncology research and provide cutting-edge treatment options to patients. Research Associates at Cedars-Sinai benefit from working in a supportive, innovative, and multidisciplinary environment that prioritizes employee growth and patient outcomes equally. This role is ideal for motivated individuals seeking to advance their career in clinical research while making a meaningful contribution to groundbreaking medical discoveries and patient care excellence.
Job Requirements
- High school diploma/GED required
- Bachelor’s degree preferred
- 1 year clinical research related experience required
Job Qualifications
- High school diploma or GED required
- Bachelor’s degree preferred
- At least 1 year of clinical research related experience
- Knowledge of IRB, FDA, OHRP, and HIPAA guidelines
- Strong organizational and communication skills
- Ability to work collaboratively in a multidisciplinary team
- Detail-oriented with strong regulatory compliance focus
Job Duties
- Submits research projects for human subjects' approval
- Submits appropriate internal documentation for contract execution
- Maintains communication with contracting officers and sponsors during budgeting and negotiating
- Develops research project budgets based on protocol requirements
- Monitors study payments and generates invoices
- Ensures timely filing of annual renewals and amendments to IRB
- Maintains high quality regulatory files and documentation
Job Criteria
Experience
Entry Level (1-2 years)
Job Location
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