Clinical Research Coordinator
- Consulting
- $50 - $67
- Los Angeles, CA
Clinical Research Coordinator in Los Angeles, CA. Opportunity!
A bit about us:
Prestige Hospital System
Advancing new knowledge and improving health outcomes through research
Advancing new knowledge and improving health outcomes through research
Why join us?
Competitive compensation
Medical Insurance
Dental Insurance
Vision Insurance
Life Insurance
Flexible Schedule
Job Stability
Career growth
If you are passionate, thrive in a fast-paced environment and are ready to take your career to the next level, we would love to hear from you.
Medical Insurance
Dental Insurance
Vision Insurance
Life Insurance
Flexible Schedule
Job Stability
Career growth
If you are passionate, thrive in a fast-paced environment and are ready to take your career to the next level, we would love to hear from you.
Job Details
Job Details:
We are seeking a dynamic and experienced Consulting Clinical Research Coordinator (CRC) to join our growing team in the healthcare industry. This role is instrumental in driving the success of diverse clinical trial types, including Phase I-IV Industry, NIH, and investigator-initiated Interventional and observational studies. The ideal candidate will have a strong background in clinical research and a proven track record of excellence in a senior or lead CRC capacity. Experience in academic medical centers, particularly UCLA/UCSF-type environments, will be highly advantageous. This role requires frequent interaction with sponsors, so comfort and experience in this area are essential.
Responsibilities:
As a Consulting Clinical Research Coordinator, your key responsibilities will include:
1. Overseeing and coordinating the daily activities of clinical trials to ensure compliance with protocol and overall clinical objectives.
2. Developing and implementing study-specific procedures, data collection systems, and research tools.
3. Collaborating with investigators to identify problems and provide solutions that ensure the integrity of research data.
4. Training and supervising clinical research staff to ensure they are performing their roles effectively and in compliance with study protocols.
5. Liaising with sponsors, investigators, and other stakeholders to ensure smooth communication and timely resolution of any issues.
6. Assisting in the preparation of regulatory submissions, progress reports, and other essential documents.
7. Participating in study design and protocol development, bringing your expertise to bear on the development of high-quality, efficient, and ethical clinical trials.
Qualifications:
To be considered for this role, you will need:
1. A minimum of 5 years of experience in a senior or lead CRC capacity, with demonstrated success in managing complex clinical trials.
2. Extensive experience across diverse trial types: Phase I–IV Industry, NIH, and investigator-initiated Interventional and observational studies.
3. Experience in academic medical centers, with a preference for UCLA/UCSF-type environments.
4. Exceptional communication skills and the ability to comfortably interact with sponsors, investigators, and other stakeholders.
5. Strong leadership and team management skills, with the ability to mentor and develop clinical research staff.
6. Excellent problem-solving skills, with the ability to identify and resolve issues in a timely and effective manner.
7. A strong commitment to ethical practices in clinical research, with a thorough understanding of regulatory requirements and guidelines.
Join us as we continue to advance the frontiers of healthcare through clinical research. We look forward to reviewing your application.
We are seeking a dynamic and experienced Consulting Clinical Research Coordinator (CRC) to join our growing team in the healthcare industry. This role is instrumental in driving the success of diverse clinical trial types, including Phase I-IV Industry, NIH, and investigator-initiated Interventional and observational studies. The ideal candidate will have a strong background in clinical research and a proven track record of excellence in a senior or lead CRC capacity. Experience in academic medical centers, particularly UCLA/UCSF-type environments, will be highly advantageous. This role requires frequent interaction with sponsors, so comfort and experience in this area are essential.
Responsibilities:
As a Consulting Clinical Research Coordinator, your key responsibilities will include:
1. Overseeing and coordinating the daily activities of clinical trials to ensure compliance with protocol and overall clinical objectives.
2. Developing and implementing study-specific procedures, data collection systems, and research tools.
3. Collaborating with investigators to identify problems and provide solutions that ensure the integrity of research data.
4. Training and supervising clinical research staff to ensure they are performing their roles effectively and in compliance with study protocols.
5. Liaising with sponsors, investigators, and other stakeholders to ensure smooth communication and timely resolution of any issues.
6. Assisting in the preparation of regulatory submissions, progress reports, and other essential documents.
7. Participating in study design and protocol development, bringing your expertise to bear on the development of high-quality, efficient, and ethical clinical trials.
Qualifications:
To be considered for this role, you will need:
1. A minimum of 5 years of experience in a senior or lead CRC capacity, with demonstrated success in managing complex clinical trials.
2. Extensive experience across diverse trial types: Phase I–IV Industry, NIH, and investigator-initiated Interventional and observational studies.
3. Experience in academic medical centers, with a preference for UCLA/UCSF-type environments.
4. Exceptional communication skills and the ability to comfortably interact with sponsors, investigators, and other stakeholders.
5. Strong leadership and team management skills, with the ability to mentor and develop clinical research staff.
6. Excellent problem-solving skills, with the ability to identify and resolve issues in a timely and effective manner.
7. A strong commitment to ethical practices in clinical research, with a thorough understanding of regulatory requirements and guidelines.
Join us as we continue to advance the frontiers of healthcare through clinical research. We look forward to reviewing your application.
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Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.
Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal.
By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here: jobot.com/privacy-policy