Clinical Trial Manager
Irvine, CA · On-site
Your Role on the Team The Clinical Trial Manager will serve as the senior scientific leader responsible for designing, developing, and overseeing high-quality clinical research programs across the ...
Irvine, CA · On-site
Your Role on the Team The Clinical Trial Manager will serve as the senior scientific leader responsible for designing, developing, and overseeing high-quality clinical research programs across the ...
Irvine, CA · On-site
Your Role on the Team The Clinical Trial Manager will serve as the senior scientific leader responsible for designing, developing, and overseeing high-quality clinical research programs across the ...
Irvine, CA · On-site
Clinical Trial Coordinator Job Responsibilities: * Provides Trial Management Filing (TMF) system support, including document inspection, filing, and auditing. * Supports study budget negotiation and ...
Irvine, CA · On-site
Clinical Trial Coordinator Job Responsibilities: * Provides Trial Management Filing (TMF) system support, including document inspection, filing, and auditing. * Supports study budget negotiation and ...
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
New
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
New
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
New
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
New
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
New
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
New
Nephrologist(Clinical Trial) - Pomona, CA Compensation: $100-$200/hr or based on market standard rates Commitment: 0-8 hours/weekStart Date: Within 0-6 months Position Summary We are seeking a board ...
Nephrologist(Clinical Trial) - Pomona, CA Compensation: $100-$200/hr or based on market standard rates Commitment: 0-8 hours/weekStart Date: Within 0-6 months Position Summary We are seeking a board ...
Psychiatrist (Clinical Trial) - Part Time- Pomona, CA Job Type: Part Time Shifts: 0-8 hours/week Key Responsibilities: * Serve as Sub-Investigator or Principal Investigator in clinical trials.
Psychiatrist (Clinical Trial) - Part Time- Pomona, CA Job Type: Part Time Shifts: 0-8 hours/week Key Responsibilities: * Serve as Sub-Investigator or Principal Investigator in clinical trials.
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
New
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
New
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
New
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
New
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
New
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10-16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics ...
New
Psychiatrist (Clinical Trial Physician) - Tustin, CA Job Type: Part-Time (0-8 hours/week) Job Summary & Responsibilities: * Serve as Principal Investigator or Sub-Investigator in clinical trials.
Psychiatrist (Clinical Trial Physician) - Tustin, CA Job Type: Part-Time (0-8 hours/week) Job Summary & Responsibilities: * Serve as Principal Investigator or Sub-Investigator in clinical trials.
Pomona, CA · On-site
$100 - $200/hr
Gastroenterologist (Clinical Trial Physician) Location: Inland Clinical Research Address: Pomona, CA Commitment: 0-8 hours/week Start Date: Within 0-6 months Compensation: $100-$200/hr or based on ...
Pomona, CA · On-site
$100 - $200/hr
Gastroenterologist (Clinical Trial Physician) Location: Inland Clinical Research Address: Pomona, CA Commitment: 0-8 hours/week Start Date: Within 0-6 months Compensation: $100-$200/hr or based on ...
Gastroenterologist (Clinical Trial Physician) Location: Inland Clinical Research Address: Pomona, CA Commitment: 0-8 hours/week Start Date: Within 0-6 months Compensation: $100-$200/hr or based on ...
Gastroenterologist (Clinical Trial Physician) Location: Inland Clinical Research Address: Pomona, CA Commitment: 0-8 hours/week Start Date: Within 0-6 months Compensation: $100-$200/hr or based on ...
Pomona, CA · On-site
$100 - $200/hr
Obesity Medicine Specialist (Clinical Trial Physician) - Pomona, CA Job Type: Part-Time Shift: Day Position Summary: We are seeking a board-certified Obesity Medicine Specialist to serve as a ...
Pomona, CA · On-site
$100 - $200/hr
Obesity Medicine Specialist (Clinical Trial Physician) - Pomona, CA Job Type: Part-Time Shift: Day Position Summary: We are seeking a board-certified Obesity Medicine Specialist to serve as a ...
Irvine, CA · On-site
$30 - $40/hr
Irvine Clinical Research is the largest independent clinical trial group on the West Coast. We're expanding our research in GLP-1 and incretins, testing the efficacy and safety of investigational ...
Quick apply
Irvine, CA · On-site
$30 - $40/hr
Irvine Clinical Research is the largest independent clinical trial group on the West Coast. We're expanding our research in GLP-1 and incretins, testing the efficacy and safety of investigational ...
Irvine Clinical Research is the largest independent clinical trial group on the West Coast. We're expanding our research in GLP-1 and incretins, testing the efficacy and safety of investigational ...
Irvine Clinical Research is the largest independent clinical trial group on the West Coast. We're expanding our research in GLP-1 and incretins, testing the efficacy and safety of investigational ...
Riverside, CA · On-site
$30 - $40/hr
Irvine Clinical Research is the largest independent clinical trial group on the West Coast. We're expanding our research in GLP-1 and incretins, testing the efficacy and safety of investigational ...
Quick apply
Riverside, CA · On-site
$30 - $40/hr
Irvine Clinical Research is the largest independent clinical trial group on the West Coast. We're expanding our research in GLP-1 and incretins, testing the efficacy and safety of investigational ...
Irvine Clinical Research is the largest independent clinical trial group on the West Coast. We're expanding our research in GLP-1 and incretins, testing the efficacy and safety of investigational ...
Irvine Clinical Research is the largest independent clinical trial group on the West Coast. We're expanding our research in GLP-1 and incretins, testing the efficacy and safety of investigational ...
Irvine, CA · On-site
$100K/yr
Contribute to clinical aspects of protocol development; specifically develop the Safety section of clinical trial protocols including adverse event definitions, AE reporting requirements, and risk ...
Irvine, CA · On-site
$100K/yr
Contribute to clinical aspects of protocol development; specifically develop the Safety section of clinical trial protocols including adverse event definitions, AE reporting requirements, and risk ...
Contribute to clinical aspects of protocol development; specifically develop the Safety section of clinical trial protocols including adverse event definitions, AE reporting requirements, and risk ...
Contribute to clinical aspects of protocol development; specifically develop the Safety section of clinical trial protocols including adverse event definitions, AE reporting requirements, and risk ...
$30.09 - $36.48
4% of jobs
$36.48 - $42.86
6% of jobs
$42.86 - $49.25
7% of jobs
$54.03 is the 25th percentile. Wages below this are outliers.
$49.25 - $55.63
9% of jobs
$55.63 - $62.01
15% of jobs
The median wage is $64.83 / hr.
$62.01 - $68.40
18% of jobs
$72.94 is the 75th percentile. Wages above this are outliers.
$68.40 - $74.78
21% of jobs
$74.78 - $81.16
7% of jobs
$81.16 - $87.55
6% of jobs
$87.55 - $93.93
3% of jobs
$93.93 - $100.31
2% of jobs
$30
$65
$100

Other
Medical, Retirement, PTO
Posted 7 days ago
8.7
Based on 41 frontline employees who took The Breakroom Quiz
56th of 611 rated colleges and universities
Founded in 1965, UC Irvine is a member of the prestigious Association of American Universities and is ranked among the nation's top 10 public universities by U.S. News & World Report. The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs. It's located in one of the world's safest and most economically vibrant communities and is Orange County's second-largest employer, contributing $7 billion annually to the local economy and $8 billion statewide.
To learn more about UC Irvine, visit www.uci.edu.
The Susan Samueli Integrative Health Institute (SSIHI), part of UCI Health and the Susan & Henry College of Health Sciences, works to transform healthcare through the practice of integrative health by conducting rigorous research, promoting evidence-based treatment modalities, educating the public on well-being practices, providing individualized, patient-centered clinical care, and providing services to the community that focus on obtaining optimal health.
The Clinical Trial Manager will serve as the senior scientific leader responsible for designing, developing, and overseeing high-quality clinical research programs across the Susan Samueli Integrative Health Institute (SSIHI), while strategically guiding industry sponsors, faculty, and research teams, through successful partnerships with the University of California, Irvine (UCI). This individual will bring deep expertise in clinical trial methodology, protocol development, regulatory strategy, and academic-industry collaboration, with working knowledge of machine learning and artificial intelligence applications in clinical research. The role will lead protocol conception and authorship, support sponsor engagement and feasibility, ensure scientific rigor and operational feasibility, and oversee research program outcomes to drive measurable impact, publication quality, funding growth, and translational value. The Principal Clinical Trial Manager will collaborate closely with investigators, federal regulatory agencies, data science partners, IT and compliance teams, and external sponsors to ensure responsible integration and advanced analytics into SSIHI's clinical research programs, including predictive modeling, digital biomarkers, real-world data, and decision-support applications.
Required:
Preferred:
Total Rewards
In addition to the salary range listed below, we offer a wealth of benefits to make working at UCI even more rewarding. These benefits may include medical insurance, sick and vacation time, retirement savings plans, and access to a number of discounts and perks. Please utilize the links listed here to learn more about our compensation practices and benefits.
Conditions of Employment:
The University of California, Irvine (UCI) seeks to provide a safe and healthy environment for the entire UCI community. As part of this commitment, all applicants who accept an offer of employment must comply with the following conditions of employment:
*Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.
The following additional conditions may apply, some of which are dependent upon business unit or job specific requirements.
Details of each policy may be reviewed by visiting the following page - https://hr.uci.edu/new-hire/conditions-of-employment.php
Closing Statement:
The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the UC Anti-Discrimination Policy.
We are committed to attracting and retaining a diverse workforce along with honoring unique experiences, perspectives, and identities. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable, and welcoming.
UCI provides reasonable accommodations for applicants with disabilities upon request. For more information, please contact Human Resources at (949) 824-0500 or eec@uci.edu.
Get the full story on Breakroom
Sourced by ZipRecruiter