Clinical Research Associate (CRA)
Location: Los Angeles, CA
Job Type: Contract To Hire
Company: IDR
Category: All Other
Job Description Apply Now
The Clinical Research Associate (CRA) plays a critical role in supporting clinical research initiatives by working onsite with a dedicated team to ensure the smooth execution of research studies. As a Clinical Research Associate (CRA), you will be immersed in a dynamic environment, collaborating closely with research professionals to advance scientific discovery and medical innovation. This full-time position offers the opportunity to be part of a reputable organization recognized for its industry leadership and commitment to high-quality research. If you are passionate about clinical research and eager to contribute to groundbreaking projects, consider applying for the Clinical Research Associate (CRA) role today.
As a Clinical Research Associate (CRA), you will be responsible for coordinating a variety of research activities. Your primary duties include facilitating the submission of research projects for human subjects approval, managing essential documentation, and ensuring regulatory compliance throughout the research lifecycle. Working with both internal teams and external partners, you will help develop and monitor budgets, coordinate site visits, and maintain clear communication with sponsors and investigators. Your attention to detail and organizational skills will be crucial for managing regulatory files, preparing necessary paperwork, and upholding the highest standards of compliance with IRB, FDA, OHRP, HIPAA, and related guidelines.
The Clinical Research Associate (CRA) role requires a strong foundation in research protocols and documentation. Candidates should possess excellent communication abilities, the capacity to work collaboratively across multidisciplinary teams, and a keen eye for detail. Previous experience in clinical research—especially in fields such as oncology, chemotherapy, or pharmaceuticals—is highly valued. A high school diploma or GED is required, while a bachelor’s degree is preferred. If you are looking to develop your career within a supportive, team-oriented environment and gain exposure to industry-leading practices, the Clinical Research Associate (CRA) position presents an exceptional opportunity.
The organization offers a comprehensive benefits package, opportunities for career advancement, and a culture that values collaboration, innovation, and professional growth. Employees benefit from a competitive compensation structure, access to medical, dental, and vision coverage, and participation in programs like Employee Stock Ownership. The team’s collective expertise and dedication have earned industry accolades, including multiple Best of Staffing® Client and Talent Awards. Working as a Clinical Research Associate (CRA) allows you to make meaningful contributions to the field of clinical research while enjoying a positive and inclusive work environment.
Located in Los Angeles, CA, this position allows you to engage with a diverse and vibrant research community, leveraging the area’s resources and network of professionals. The Clinical Research Associate (CRA) role is designed for individuals who thrive in fast-paced settings and are committed to advancing research excellence. If you are ready to take the next step in your clinical research career, click the application button and join a team that is shaping the future of healthcare and scientific discovery.
Clinical Research Associate (CRA) - Summary- Full-time position supporting onsite clinical research operations
- Key responsibilities include regulatory compliance, documentation management, and coordination of research activities
- Opportunity to collaborate with seasoned professionals in a dynamic, industry-leading organization
- Work in Los Angeles, CA, and contribute to impactful medical research initiatives
- Collaborate with research teams to submit projects for human subjects approval, including protocols, consent forms, and IRB applications
- Manage and maintain internal documentation for contract execution
- Communicate with contracting officers and sponsors during budgeting and negotiation phases
- Develop and monitor research project budgets, ensuring compliance with protocol and institutional requirements
- Maintain high-quality regulatory files and submit required paperwork in accordance with IRB, FDA, OHRP, HIPAA, and other guidelines
- Coordinate site feasibility and initiation visits; provide facility tours for sponsors and personnel
- Foster collaboration among internal teams, investigators, and participating research centers
- Competitive compensation package
- Comprehensive benefits including medical, dental, vision, and life insurance
- Employee Stock Ownership Program
- Access to professional development and career growth opportunities
- Recognition through industry awards and a supportive, team-oriented culture
- High School Diploma or GED required; Bachelor’s degree preferred
- Minimum one year of experience in clinical research (chemo, oncology, or pharmaceutical research preferred)
- Strong organizational and documentation skills
- Attention to detail in all aspects of regulatory compliance and research management
- Effective collaboration and communication skills with both internal and external stakeholders
- Motivated, detail-oriented professional with a passion for clinical research
- Able to manage multiple research projects and adapt to a fast-paced environment
- Strong commitment to regulatory compliance and ethical research practices
- Interest in advancing within the clinical research field
- Be part of a team with over 25 years of industry experience and a track record of excellence
- Opportunity to work in a vibrant and resource-rich location
- Inclusive workplace that values diversity and equal opportunity
- Employees are encouraged to self-identify for voluntary compliance with civil rights regulations
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. IDR is subject to certain governmental recordkeeping and reporting requirements for the administration of civil rights laws and regulations. In order to comply with these laws, we invite employees to voluntarily self-identify their race or ethnicity, gender, and veteran status (if applicable). Submission of this information is voluntary and refusal to provide it will not subject you to any adverse treatment. The information obtained will be kept confidential and may only be used in accordance with the provisions of applicable laws, executive orders, and regulations, including those that require the information to be summarized and reported to the federal government for civil rights enforcement. You may access this form here.
If you are ready to advance your career as a Clinical Research Associate (CRA), click the application button to apply today and become a valued member of a forward-thinking clinical research team.