Top 20 Director of regulatory affairs Jobs in Riverside Ca

Senior Director, Oncology Pharmacology
Jazz Pharmaceuticals —California
- $232,000 - $348,000 a year
- Analysis skills
- Doctor of Philosophy
- Mentoring
- Health insurance
- Dental insurance
Government Affairs Analyst I/II (DOQ)
Inland Empire Utilities Agency —Chino, CA
- $120,456.18 - $161,812.30 a year
- Full-time
- Mid-level
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- Bachelor's degree
- Profit sharing
- AD&D insurance
1d
Neuroscience Therapeutic Sales Specialist (Riverside, CA)
Compass Pathways —Riverside, CA
- $165,000 - $195,000 a year
- Call employer
- Remote
- Bachelor's degree
- Travel
- Senior level
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2d
Executive Director (SMSU)
California State University —San Bernardino, CA
- Extended hours
- Background check
- Office
- Master's degree
- AD&D insurance
- Disability insurance
FSQA Beef Technical Services Manager
In-N-Out —Chino, CA
- $127,000 - $150,000 a year
- Weekends as needed
- Up to 50% travel
- 5 years
- Master's degree
- Profit sharing
- Health insurance
4d
Athletics Administrative Analyst (Administrative Analyst/Specialist Exempt II), Athletics
California State University —San Bernardino, CA
- Full-time
- Background check
- Office
- Administrative experience
- Paid holidays
- Health insurance
1d
Associate Product Development Project Manager
Developlus, Inc. —Corona, CA
- $85,000 - $110,000 a year
- Hybrid work
- Marketing
- Bachelor's degree
- Continuous improvement
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5d
Assistant Director of Licensure and Compliance
University of Redlands —Redlands, CA
- $70,304 a year
- Weekends as needed
- Background check
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- 5 years
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Respiratory Therapy Instructor
Carrington College —Ontario, CA
- $35 - $40 an hour
- Part-time
- Background check
- Classroom
- Microsoft Excel
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Special Programs Manager I - Commercial Products
Inland Empire Health Plan —Rancho Cucamonga, CA
- $80,059.20 - $106,059.20 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Disability insurance
- Health insurance
Faculty Program and Continuing Medical Education Specialist
California University Of Science And Medicine —Colton, CA
- $65,000 - $75,000 a year
- Full-time
- Microsoft Outlook
- Mid-level
- Office
Quick Apply
Nursing Clinical Instructor
Carrington College —Ontario, CA
- $58 - $70 an hour
- Part-time
- Background check
- Classroom
- Nursing
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Operations & Collections Specialist
University of Redlands —Redlands, CA
- $25 - $30 an hour
- Full-time
- Background check
- Microsoft Outlook
- Computer literacy
Quick Apply
Sr. Director, Consumer Marketing
ZO Skin Health, Inc —Irvine, CA
- Hybrid work
- Marketing
- Office
- Bachelor's degree
Quick Apply
21h
Dietitian (Clinical) (Community Based Outpatient Clinic-Rancho Cucamonga
US Veterans Health Administration —Rancho Cucamonga, CA
- $93,141 - $121,089 a year
- Online Application
- Background check
- Pass drug screening
- English
1d
Research Associate
Western University of Health Sciences —Pomona, CA
- $17 an hour
- Weekends as needed
- Background check
- Bachelor of Science
- Mid-level
- Paid time off
- Retirement plan
Clinic Medical Director
OneTogether Solutions —Perris, CA
- $300,000 - $375,000 a year
- Full-time
- Medicine
- 7 years
- Patient monitoring
- On-the-job training
- Opportunities for advancement
Quick Apply
6d
Senior Manager/Associate Director, Regulatory CMC Consultant (REMOTE)
Kaztronix —United States
- Contract
- Remote
- 6 years
- Management
- Bachelor's degree
Quick Apply

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Senior Director, Oncology Pharmacology

Jazz Pharmaceuticals -
California

Apply Now

Job Details

$232,000 - $348,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Vision insurance

Qualifications

FDA submissions
Experimental data reports
Program design
GLP
Clinical study protocols and reports
Molecular biomarkers
Competitive analysis
Technical report writing
In vitro studies
Investigational new drug (IND) applications
Team development
Pre-clinical study projects
Managing teams of scientists
Doctor of Philosophy
Scientific protocols
Compliance documentation
Mentoring
Leading team collaboration initiatives
Experimental design
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials
In vivo studies
Technical project management
GraphPad Prism
Oncology
Clinical research reports
Clinical data analysis
Translational research
Cross-functional team management
Pharmaceutical research experience

Full Job Description

If you are a current Jazz employee please apply via the Internal Career site.

Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.

Brief Description

This individual will be responsible for leading scientific team members assigned to oncology assets ranging from discovery through regulatory approval.
This individual will both manage the oncology pharmacology team and serve a lead on one or more programs themselves.
Primary responsibilities of the oncology pharmacology team include establishing efficacy in relevant disease models, demonstrating differentiation relative to relevant comparators, determining PK/PD/efficacy relationships, characterizing mechanisms of action, identifying predictive disease models, indications, and biomarkers, driving preclinical discovery, supporting research and development of Jazz products and drug candidates overall, and designing and executing studies that address clinically relevant priorities.
Operational tasks include designing and executing experiments that are outsourced or performed by in-house bench researchers or academic collaborators, reviewing and contributing to clinical protocols, reviewing and authoring technical reports, coauthoring sections of regulatory documents ranging from IND to NDA/BLA submissions, and communicating relevant research at internal and external forums.
The oncology pharmacology team cross-functional, including participation in matrix teams assigned to specific products that include but are not limited to Clinical Development, Bioanalytical, Toxicology, Clinical Pharmacology, Biomarkers Regulatory Affairs, and Project Management.
Collaborate with and represent ORP on internal teams—to design, develop, implement, and oversee execution of strategies and experiments supporting nonclinical studies in hematologic malignancies and solid tumors.

Essential Functions

Design and execute experiments to elucidate efficacy, tolerability, mechanism of action, and biomarkers associated with complex combinations of multiple therapeutic modalities (small molecules, biologics, ADCs, bi-specifics, cell therapies, and other emerging platforms).
Critically evaluate biochemical and cellular assays.
Communicate effectively across JAZZ functional teams, highly matrixed, cross functional environments.
Demonstrate strong interpersonal, negotiation, and influence skills.
Independently develop experimental strategies, analyze data, and present results to non‑clinical and governance-level teams.
Collaborate with CROs to outsource studies, develop protocols, manage timelines and budgets, and partner with academic labs for Jazz sponsored research.
Serve as a project team leader and/or as lead pharmacology representative across various oncology programs,
Mentor junior scientists and providing scientific leadership and professional growth opportunities.

Required Knowledge, Skills, and Abilities

Industry experience evaluating therapeutic potential of drug candidates from hit to lead optimization through IND enabling studies, with deep expertise in oncology drug development.
Broad background in preclinical oncology with strong familiarity with emerging therapeutic modalities, competitive landscapes, and strategic assessment of diverse drug mechanisms.
Extensive experience in Immuno Oncology (I/O), including I/O relevant in vivo and in vitro models, immune cell biology, and integration of immunological endpoints into pharmacology programs.
Demonstrated experience working across multiple drug modalities, including small molecules, biologics, ADCs, bi-specifics, T cell engagers, cell and gene therapies, and RNA based therapeutics.
Strong foundational understanding of the interdependencies between Nonclinical Pharmacology, Toxicology, DMPK, and Clinical Pharmacology, including how these functions integrate to enable successful dose selection, therapeutic index characterization, risk assessment, and translational strategy.
Deep understanding of cancer signaling pathways and their therapeutic exploitation.
Proven experience leading multiple complex pharmacology programs at diverse CROs, including GLP and non-GLP environments.
Expertise designing and executing studies evaluating efficacy, tolerability, mechanism of action, and biomarker strategies for small molecule and biologic agents.
Ability to integrate preclinical and clinical datasets, innovate, and apply novel methodologies to advance therapeutic programs.
Proficiency with analytical tools (e.g., GraphPad Prism) and biomarker data analysis.
Direct people management experience, including mentorship, performance development, and leadership of scientific teams.
Strong leadership qualities, self motivation, and demonstrated success networking across internal teams, academia, industry, and regulatory agencies.
Excellent ability to assess program needs, oversee CRO activities, develop/review protocols, monitor execution, interpret results, and prepare high quality reports for regulatory submissions.
Experience authoring nonclinical components of IND, NDA/BLA/MAA submissions, briefing packages, DSURs, IBs, and fast track designation documents, with proven ability to ensure alignment and scientific rigor.
Strong project management skills with the ability to manage multiple complex programs simultaneously.
Demonstrated success leading in fast paced, highly matrixed environments, aligning diverse stakeholders and driving decision making.
Strong analytical and creative problem-solving skills.
Embody and model Jazz core values.

Required/Preferred Education and Licenses

Ph.D. in biology, biochemistry, immunology, pharmacology, or a related discipline, with experience leading early oncology programs and developing nonclinical models for characterizing therapeutic efficacy and pharmacodynamics, including substantial oncology and immuno-oncology experience.

#LI-SM1

#LI-remote

Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.

FOR US BASED CANDIDATES ONLY

Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $232,000.00 - $348,000.00

Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis.

At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.

The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html.

Apply Now

Refine Your Search

director of regulatory affairs jobs in riverside ca

Senior Director, Oncology Pharmacology

Government Affairs Analyst I/II (DOQ)

Neuroscience Therapeutic Sales Specialist (Riverside, CA)

Executive Director (SMSU)

FSQA Beef Technical Services Manager

Athletics Administrative Analyst (Administrative Analyst/Specialist Exempt II), Athletics

Associate Product Development Project Manager

Assistant Director of Licensure and Compliance

Respiratory Therapy Instructor

Special Programs Manager I - Commercial Products

Faculty Program and Continuing Medical Education Specialist

Nursing Clinical Instructor

Operations & Collections Specialist

Sr. Director, Consumer Marketing

Dietitian (Clinical) (Community Based Outpatient Clinic-Rancho Cucamonga

Research Associate

Clinic Medical Director

Senior Manager/Associate Director, Regulatory CMC Consultant (REMOTE)

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