Experience supporting product development and lifecycle management Clinical Research Leadership * Led clinical studies or clinical programs, not just participated in them * Experience designing ...
New
Experience supporting product development and lifecycle management Clinical Research Leadership * Led clinical studies or clinical programs, not just participated in them * Experience designing ...
New
Experience supporting product development and lifecycle management Clinical Research Leadership * Led clinical studies or clinical programs, not just participated in them * Experience designing ...
New
Irvine, CA · On-site
$145K/yr
Manager, Clinical Research Affairs Role Level: People Manager Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA - Corporate office environment Summary: The ...
Irvine, CA · On-site
$145K/yr
Manager, Clinical Research Affairs Role Level: People Manager Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA - Corporate office environment Summary: The ...
Manager, Clinical Research Affairs Role Level: People Manager Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA - Corporate office environment Summary: The ...
Manager, Clinical Research Affairs Role Level: People Manager Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA - Corporate office environment Summary: The ...
Serve as a Clinical Research Lead to execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones, for Biosense Webster. * Oversight/execution of ...
Serve as a Clinical Research Lead to execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones, for Biosense Webster. * Oversight/execution of ...
Irvine, CA · On-site
Serve as a Clinical Research Lead to execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones, for Biosense Webster. * Oversight/execution of ...
Irvine, CA · On-site
Serve as a Clinical Research Lead to execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones, for Biosense Webster. * Oversight/execution of ...
Irvine, CA · On-site
Serve as a Clinical Research Lead to execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones, for Biosense Webster. * Oversight/execution of ...
Irvine, CA · On-site
Serve as a Clinical Research Lead to execute and manage company sponsored clinical trials, ensuring compliance with timelines and study milestones, for Biosense Webster. * Oversight/execution of ...
Santa Ana, CA · On-site
$65 - $70/hr
Southern California Clinical Research part of Southern California Dermatology clinic in Santa Ana ... The Candidate will also be responsible for educating patients about their treatment and managing ...
Santa Ana, CA · On-site
$65 - $70/hr
Southern California Clinical Research part of Southern California Dermatology clinic in Santa Ana ... The Candidate will also be responsible for educating patients about their treatment and managing ...
Murrieta, CA · On-site
$31 - $38/hr
Additional duties as assigned by management. Required Skills * Must have oncology clinical research experience * Minimum of two years of clinical research experience Preferred Skills * Bachelor ...
Murrieta, CA · On-site
$31 - $38/hr
Additional duties as assigned by management. Required Skills * Must have oncology clinical research experience * Minimum of two years of clinical research experience Preferred Skills * Bachelor ...
Proven ability to work independently, manage multiple projects simultaneously, and meet aggressive ... Total Rewards program. We are committed to attracting and retaining high quality talent by ...
Proven ability to work independently, manage multiple projects simultaneously, and meet aggressive ... Total Rewards program. We are committed to attracting and retaining high quality talent by ...
Proven ability to work independently, manage multiple projects simultaneously, and meet aggressive ... Total Rewards program. We are committed to attracting and retaining high quality talent by ...
Proven ability to work independently, manage multiple projects simultaneously, and meet aggressive ... Total Rewards program. We are committed to attracting and retaining high quality talent by ...
Manage with supervision clinical trials including study budget assessment, fair mark value ... Ensure clinical research studies follow regulatory standards and maintain accurate, detailed ...
Manage with supervision clinical trials including study budget assessment, fair mark value ... Ensure clinical research studies follow regulatory standards and maintain accurate, detailed ...
Manage with supervision clinical trials including study budget assessment, fair mark value ... Ensure clinical research studies follow regulatory standards and maintain accurate, detailed ...
Manage with supervision clinical trials including study budget assessment, fair mark value ... Ensure clinical research studies follow regulatory standards and maintain accurate, detailed ...
Individual Contributor (IC) Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA, Corporate Office Summary: The Senior Clinical Research Associate will report ...
Individual Contributor (IC) Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA, Corporate Office Summary: The Senior Clinical Research Associate will report ...
Anaheim, CA · On-site
$200 - $300/hr
We partner closely with physicians to build high-quality, scalable clinical research programs that advance patient care while creating long-term professional and financial opportunities for our ...
Quick apply
Anaheim, CA · On-site
$200 - $300/hr
We partner closely with physicians to build high-quality, scalable clinical research programs that advance patient care while creating long-term professional and financial opportunities for our ...
Irvine, CA · On-site
$95K/yr
Individual Contributor (IC) Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA, Corporate Office Summary: The Senior Clinical Research Associate will report ...
Irvine, CA · On-site
$95K/yr
Individual Contributor (IC) Supervisor/Manager Title: Director, Clinical Affairs Job Location & Environment: Irvine, CA, Corporate Office Summary: The Senior Clinical Research Associate will report ...
Murrieta, CA · On-site
$21 - $32/hr
... management Requirements * Bachelor's degree preferred, but not required * Clinical research ... leave, referral program, employee assistance program, life insurance, disability insurance ...
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Murrieta, CA · On-site
$21 - $32/hr
... management Requirements * Bachelor's degree preferred, but not required * Clinical research ... leave, referral program, employee assistance program, life insurance, disability insurance ...
Murrieta, CA · On-site
$21 - $32/hr
... management Requirements * Bachelor's degree preferred, but not required * Clinical research ... leave, referral program, employee assistance program, life insurance, disability insurance ...
Murrieta, CA · On-site
$21 - $32/hr
... management Requirements * Bachelor's degree preferred, but not required * Clinical research ... leave, referral program, employee assistance program, life insurance, disability insurance ...
Murrieta, CA · On-site
$21 - $32/hr
... management Requirements * Bachelor's degree preferred, but not required * Clinical research ... leave, referral program, employee assistance program, life insurance, disability insurance ...
Murrieta, CA · On-site
$21 - $32/hr
... management Requirements * Bachelor's degree preferred, but not required * Clinical research ... leave, referral program, employee assistance program, life insurance, disability insurance ...
Irvine, CA · On-site
$18 - $32/hr
National Institute of Clinical Research, a research organization serving the pharmaceutical and ... The ability and willingness to learn new software programs is also required. QUALIFICATIONS Medical ...
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Irvine, CA · On-site
$18 - $32/hr
National Institute of Clinical Research, a research organization serving the pharmaceutical and ... The ability and willingness to learn new software programs is also required. QUALIFICATIONS Medical ...
Irvine, CA · On-site
$18 - $32/hr
National Institute of Clinical Research, a research organization serving the pharmaceutical and ... The ability and willingness to learn new software programs is also required. QUALIFICATIONS Medical ...
Quick apply
Irvine, CA · On-site
$18 - $32/hr
National Institute of Clinical Research, a research organization serving the pharmaceutical and ... The ability and willingness to learn new software programs is also required. QUALIFICATIONS Medical ...
$46.4K - $56.4K
2% of jobs
$56.4K - $66.3K
12% of jobs
$75.8K is the 25th percentile. Wages below this are outliers.
$66.3K - $76.3K
12% of jobs
$76.3K - $86.3K
20% of jobs
The median wage is $88.6K / yr.
$86.3K - $96.2K
18% of jobs
$104.3K is the 75th percentile. Wages above this are outliers.
$96.2K - $106.2K
14% of jobs
$106.2K - $116.1K
5% of jobs
$116.1K - $126.1K
9% of jobs
$126.1K - $136.1K
4% of jobs
$136.1K - $146K
3% of jobs
$146K - $156K
1% of jobs
$46.4K
$96.6K
$156K
| Aspect | Clinical Research Program Manager | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's or higher in life sciences, often with project management certifications | Typically holds a bachelor's degree in health sciences or related field |
| Work Environment | Oversees multiple studies, manages teams, and coordinates with stakeholders | Handles daily study activities, patient interactions, and data collection |
| Employer & Industry Usage | Pharmaceutical companies, CROs, academic institutions | Hospitals, clinics, research sites |
| Search & Comparison Intent | Focuses on management, oversight, and program coordination | Focuses on study-specific tasks and patient management |
The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.
For Clinical Research Program Manager jobs in Riverside, CA, the most frequently searched job titles are:
The top searched job categories for Clinical Research Program Manager jobs in Riverside, CA are:
Cities near Riverside, CA with the most Clinical Research Program Manager job openings:
Full-time
Medical, Vision, Life, Retirement, PTO
Posted 2 days ago
New
8.3
Based on 112 frontline employees who took The Breakroom Quiz
25th of 86 rated pharmaceutical
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Discovery & Pre-Clinical/Clinical DevelopmentJob Sub Function:
Clinical Development & Research - Non-MDJob Category:
Scientific/TechnologyAll Job Posting Locations:
Irvine, California, United States of America, Jacksonville, Florida, United States of America, Milpitas, California, United States of AmericaJob Description:
JOB POSITION SUMMARY
Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of vision treatments? Ready to join a team that's reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life. Our products and services address these needs - from the pediatric to aging eye - in a patient's lifetime. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
We are searching for the best talent to join our Vision team, as Principal Clinical Research Scientist , J&J Vision, located preferably in Jacksonville, FL, Milpitas, CA, or Irvine, CA.
Purpose:
The Principal Clinical Research Scientist for Vision is an expert in ophthalmic and medical device research who serves as a core team member on key projects and leads a team of Staff Clinical Scientist. This role provides strategic and scientific leadership for the development and execution of clinical programs that generate robust evidence to support innovative vision care products and technologies. Leveraging deep expertise in clinical research, product development, and ophthalmic regulations, the Principal Clinical Research Scientist influences development strategies, aligns cross-functional stakeholders, and drives successful execution of complex initiatives that improve outcomes for eye care professionals and their patients.
You will be responsible for:
Represent Clinical Science as core team member on critical projects, liaising
between project and functional teams, and coordinating with Clinical Operations
and Project Management partners to deliver on time, within budget, and in
compliance with regulations and SOPs.
Activate and build collaborative relationships with across business platforms as well as key cross-functional partners (e.g., Global Strategic Marketing, Medical Affairs, Regulatory Affairs, R&D, etc.) to ensure consistent alignment in new product development and through product life cycle.
Lead initiatives for appropriate interpretation and dissemination of all evidence generated, including Clinical Study Reports, abstracts, manuscripts, and MDR-related documents (CER, PMCF, Clinical Plans, etc.).
Contribute to clinical scientific discussions with regulatory agencies that support the clinical and regulatory strategy, including proposed investigations, review process of evidence to support marketing authorization, and support of regulatory inspections
Engage and collaborate with industry's key opinion leaders, including KOLs and regulatory agencies, and build on relationships established through professional/technical societies
Performs other related duties as assigned by management.
Qualifications / Requirements:
Education
Advanced degree in scientific discipline (required)
OD, MD/Ophthalmologist, or PhD in Vision Science/related field strongly preferred
Post-graduate training, residency, or fellowship preferred
Ophthalmic Expertise
5+ years of ophthalmic clinical research experience
Deep understanding of eye care, ophthalmic devices, vision science, or related therapeutic areas
Experience supporting product development and lifecycle management
Clinical Research Leadership
Led clinical studies or clinical programs, not just participated in them
Experience designing studies and selecting endpoints
Demonstrated leadership on complex, cross-functional projects
Technical Writing
Personally authored or substantially contributed to:
Clinical study protocols
Clinical Study Reports (CSRs)
Scientific abstracts
Manuscripts/publications
Scientific & Statistical Acumen
Can interpret study results independently
Comfortable working with biostatisticians on:
Sample size assumptions
Endpoint strategy
Statistical analysis plans
Interpretation of results
Communication & Influence
Demonstrated ability to influence without direct authority
Experience partnering with R&D, Regulatory Affairs, Marketing, Medical Affairs, and Clinical Operations
REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES AND AFFILIATIONS
Strong technical writing ability, such as clinical study protocols, reports and abstracts is required
Understanding of biostatistics as applied to study data is required
Proficient with computers and software programs is required
TRAVEL REQUIREMENTS
Up to 10% of domestic or international travel is required
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.
Required Skills:
Preferred Skills:
Clinical Evaluations, Coaching, Critical Thinking, Drug Discovery Development, Entrepreneurship, Good Clinical Practice (GCP), Leadership, Medicines and Device Development and Regulation, Organizing, Regulatory Affairs Management, Relationship Building, Research Documents, Safety-Oriented, Scientific Research, Standard Scientific Processes and Procedures, Strategic Change, Study ManagementThe anticipated base pay range for this position is :
$117,000.00 - $201,250.00For Bay Area:
$134,000.00 - $231,150.00Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k)).Get the full story on Breakroom