Clinical Research Associate

Are you a highly motivated and detail-oriented individual with a passion for clinical research? Do you want to be a part of a renowned medical center that is constantly pushing the boundaries of medical innovation? If so, then we have an exciting opportunity for you! Cedars-Sinai Medical Center is seeking a Clinical Research Associate to join our dynamic and collaborative team. In this role, you will play a crucial role in conducting clinical trials and advancing medical treatments. We are looking for someone who is dedicated, organized, and has a strong background in clinical research. If you are ready to make a meaningful impact in the field of medicine, then we encourage you to apply today!

1. Conduct clinical trials: The Clinical Research Associate will be responsible for conducting a variety of clinical trials in accordance with study protocols, regulations, and ethical guidelines.
2. Ensure compliance: It is the responsibility of the Clinical Research Associate to ensure that all research activities comply with relevant laws, regulations, and institutional policies.
3. Data collection and analysis: The incumbent will be responsible for collecting and analyzing data from clinical trials, ensuring accuracy and completeness of data.
4. Maintain accurate records: The Clinical Research Associate will be responsible for maintaining accurate and up-to-date records of all research activities, including participant information, study protocols, and regulatory documents.
5. Collaborate with team members: The role requires close collaboration with other members of the research team, including physicians, nurses, and support staff, to ensure smooth and efficient conduct of clinical trials.
6. Participant recruitment and management: The Clinical Research Associate will be responsible for recruiting and managing study participants, including obtaining informed consent, scheduling study visits, and providing study-related support.
7. Study documentation: The incumbent will be responsible for preparing and maintaining study-related documentation, including study protocols, informed consent forms, and case report forms.
8. Monitor and report adverse events: The Clinical Research Associate will be responsible for monitoring and reporting adverse events during the course of a clinical trial, in accordance with regulatory requirements.
9. Follow ethical guidelines: The role requires strict adherence to ethical guidelines and principles for the protection of human subjects participating in clinical trials.
10. Stay updated on industry developments: The incumbent will be responsible for staying updated on industry developments and advances in clinical research, and implementing new methodologies and practices as appropriate.
11. Maintain confidentiality: The Clinical Research Associate will be responsible for maintaining the confidentiality of all research-related information, in accordance with institutional policies and regulations.
12. Timely completion of tasks: The role requires timely completion of all assigned tasks, including meeting recruitment and data collection targets, and ensuring study timelines are met.
13. Quality assurance:

According to JobzMall, the average salary range for a Clinical Research Associate in Los Angeles, CA, USA is $65,000 to $95,000 per year. This can vary depending on factors such as experience, education, and the specific company or organization.

Cedars-Sinai Medical Center is a non-profit, tertiary 886-bed hospital and multi-specialty academic health science center located in Beverly Grove in the Mid-City West area of Los Angeles, California.