Clinical Research Coordinator (CRC)
Location: Los Angeles, CA
Job Type: Contract To Hire
Company: IDR
Category: All Other
Job Description Apply Now
The Clinical Research Coordinator (CRC) plays a pivotal role in the advancement of medical research by supporting both the administrative and clinical aspects of research studies. As a Clinical Research Coordinator (CRC), you will be responsible for facilitating clinical trials, ensuring regulatory compliance, and collaborating with cross-functional teams. This full-time position offers an exciting opportunity to join a reputable organization with a commitment to excellence in the field of clinical research. Working in Los Angeles, CA, you will benefit from a vibrant professional community and the chance to make a meaningful impact on patient outcomes and the future of healthcare.
As a Clinical Research Coordinator (CRC), you will engage in the design, implementation, and oversight of research projects. Your role requires comprehensive knowledge of clinical research protocols, regulatory guidelines, and patient care procedures. By joining our dynamic team, you will support vital initiatives that drive scientific discovery and contribute to the successful execution of clinical trials from Phase I to Phase IV. You will be responsible for maintaining the highest standards of quality, safety, and ethical conduct throughout every stage of the research process.
This role involves close collaboration with principal investigators, research staff, sponsors, and regulatory authorities. You will serve as a key point of contact for all study-related activities, ensuring seamless communication and efficient project management across multiple departments. Your expertise in regulatory submissions, informed consent processes, and subject recruitment will directly contribute to the success of each study and the broader mission of the organization.
In addition to your core responsibilities, you will play a strategic role in developing and implementing department-wide research initiatives. You will ensure adherence to FDA, HSPC, HIPAA, and other relevant regulations, maintaining meticulous records and documentation to support audit readiness and quality assurance. Your ability to analyze project performance, identify areas for improvement, and communicate effectively with leadership will be essential in driving continuous improvement and operational excellence.
The Clinical Research Coordinator (CRC) position in Los Angeles, CA, provides a unique opportunity to grow your career in a professionally rewarding environment. You will benefit from competitive compensation, comprehensive benefits, and the chance to work with an industry-leading organization recognized for its innovation and commitment to employee development. The organization values diversity, equity, and inclusion, ensuring all qualified applicants are considered for employment without regard to background or protected status. If you are passionate about clinical research and ready to advance your career, apply now to join our team as a Clinical Research Coordinator (CRC) in Los Angeles, CA, and make a difference in the world of healthcare.
Clinical Research Coordinator (CRC) - Summary- Full-time position supporting clinical research studies and trials from planning to execution
- Based in Los Angeles, CA, offering collaboration in a dynamic work environment
- Acts as a bridge between research teams, sponsors, and regulatory authorities
- Plays a key role in advancing scientific discovery and improving patient care
- Engage in the design and execution of clinical research projects
- Oversee aspects of research infrastructure at institutional and departmental levels
- Serve as an internal consultant, communicating project status and process improvements to leadership
- Implement department-wide initiatives, including research quality management and clinical trial recruitment
- Ensure compliance with FDA, HSPC, HIPAA, and other regulatory guidelines
- Manage consent forms, case report forms, and IRB submissions
- Coordinate research activities with principal investigators and study teams
- Monitor and report on study progress, participant safety, and data accuracy
- Support protocol writing and investigator-initiated trials
- Facilitate patient recruitment, enrollment, and follow-up
- Competitive compensation package
- Comprehensive benefits including medical, dental, vision, and life insurance
- Employee Stock Ownership Program
- Recognition as a ClearlyRated’s Best of Staffing® Client and Talent Award winner
- Opportunities for career advancement within an industry-leading organization
- Bachelor’s degree required
- Minimum of 5 years of experience in clinical research, including IRB application procedures
- Extensive experience managing Phase I-IV clinical trials
- Proficiency in protocol writing and investigator-initiated trials
- Preferred experience in pharmaceutical, biotechnology, or contract research organization (CRO) settings
- Detail-oriented and highly organized, with strong time management skills
- Excellent written and verbal communication abilities
- Ability to collaborate effectively in a team environment
- Strong knowledge of regulatory compliance requirements (FDA, HIPAA, IRB)
- Proven track record of managing multiple clinical research projects simultaneously
- This position is based in Los Angeles, CA, providing access to a dynamic and diverse professional community
- The organization values diversity, equity, and inclusion, with a commitment to providing equal employment opportunities for all qualified applicants
- Legal Disclaimer: 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. The company 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, employees may voluntarily self-identify race or ethnicity, gender, and veteran status. Submission is voluntary and refusal to provide information will not result in adverse treatment. Information will be kept confidential in accordance with applicable laws and may be used solely for civil rights enforcement.
If you are ready to take the next step in your clinical research career and contribute to impactful medical advancements, apply today for the Clinical Research Coordinator (CRC) position in Los Angeles, CA. Join a team dedicated to excellence in research and patient care!