Top 241 Research scientist Jobs in San Dimas, Ca

Pharmacovigilance Specialist
Amphastar Pharmaceuticals Inc. —Rancho Cucamonga, CA
- $110,000 - $140,000 a year
- Full-time
- Nursing
- Medicine
- Bachelor's degree
- Health savings account
- Health insurance
Quick Apply
Technical Support Scientist
Abbott Laboratories —Pomona, CA
- $81,500 - $141,300 a year
- Full-time
- Microsoft Word
- Bachelor of Science
- Research
- Health insurance
- Tuition reimbursement
Administrative Program Coordinator - Adolescent and Young Adult Program
City of Hope —Duarte, CA
- $33.80 - $52.29 an hour
- Full-time
- Mid-level
- 3 years
- Master's degree
R&D Formulator
SIRIO NUTRITION CALIFORNIA LLC —City of Industry, CA
- $90,000 - $120,000 a year
- Full-time
- Mid-level
- High school diploma or GED
- Leadership
- Paid holidays
- Health insurance
Quick Apply
3d
Research Scientist
Kerr —Pomona, CA
- $120,400 - $147,100 a year
- Microsoft Excel
- Doctoral degree
- 5 years
- Paid holidays
- Disability insurance
7h
Research Scientist
California Institute of Technology —Pasadena, CA
- $79,700 - $115,000 a year
- Full-time
- 5 years
- Machine learning
- Doctor of Philosophy
- Paid holidays
- Health insurance
1d
Senior Research Scientist
ChemEOR —Covina, CA
- Email
- Management
- Doctor of Philosophy
- Senior level
Research Associate I - Microbiome Program
City of Hope —Duarte, CA
- $27.69 - $32.12 an hour
- Full-time
- Bachelor's degree
- Entry level
- Under 1 year
3d
Research Associate II - Cancer Biology and Molecular Medicine
City of Hope —Duarte, CA
- $32.00 - $49.60 an hour
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
R&D Gummy Formulator
MeriCal, LLC —Anaheim, CA
- $85,000 - $100,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor of Science
- Wellness program
- Paid holidays
Quick Apply
Clinical Study Coordinator
City of Hope —Duarte, CA
- $44.90 - $69.60 an hour
- Full-time
- HIPAA
- Mid-level
- Bachelor's degree
Scientist II
JPL/NASA —Pasadena, CA
- $107,744 - $138,840 a year
- Full-time
- Master's degree
- Bachelor's degree
- Doctor of Philosophy
- Dental insurance
- Paid time off
R&D Laboratory Technician I
Katalyst Healthcares & Life Sciences —Brea, CA
- Contract
- Hybrid work
- Computer literacy
- Engineering
- Mid-level
Quick Apply
9d
Research Associate - Biosensing
Convergent Research —Pasadena, CA
- $65,000 - $95,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Project management
- Paid holidays
- Dental insurance
Clinical Trials Data Coord
City of Hope —Duarte, CA
- $30.67 - $47.54 an hour
- Full-time
- Remote
- HIPAA
- Mid-level
- Bachelor's degree
Research Business Manager (Remote)
City of Hope —Duarte, CA
- $45.37 - $75.77 an hour
- Full-time
- Remote
- Mid-level
- Finance
- Administrative experience
Regulatory Affairs Specialist II
City of Hope —Duarte, CA
- $40.82 - $63.27 an hour
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
8d
Scientist and R&D Manager: Antibody Products
Omnimabs —Alhambra, CA
- Mid-level
- Doctor of Philosophy
- Leadership
Research Associate II
stealth mode —Los Angeles, CA
- $75,000 - $95,000 a year
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
11d
Cognitive Scientist - AI Trainer
DataAnnotation —Garden Grove, CA
- $50 - $100 an hour
- Part-time
- Remote
- Computer Science
- English
- Mid-level
- Flexible schedule
Quick Apply

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Pharmacovigilance Specialist

Amphastar Pharmaceuticals Inc. -
Rancho Cucamonga, CA

Quick Apply

Job Details

Full-time
$110,000 - $140,000 a year

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Paid time off
401(k) matching
Life insurance
Referral program
Retirement plan

Qualifications

Database systems
Adverse event reporting
Safety regulations
ICH guidelines
Bachelor's degree
Public Health
Clinical quality assurance standards
Patient safety and incident reporting systems
Legal compliance
FDA regulations

Full Job Description

Amphastar Pharmaceuticals is seeking an experienced Pharmacovigilance professional to support and oversee global drug safety activities for marketed and investigational products. The successful candidate will be responsible for adverse event case management, safety surveillance, signal detection, regulatory compliance, and cross-functional collaboration with Clinical Development, Regulatory Affairs, Medical Affairs, Quality, and Commercial teams. This position plays a critical role in ensuring patient safety, maintaining compliance with global pharmacovigilance regulations, and supporting the continued growth of Amphastar's product portfolio.

Essential Responsibilities

Manage and oversee pharmacovigilance activities for assigned marketed and development-stage products.
Review, evaluate, and process adverse event reports in accordance with FDA, ICH, and global regulatory requirements.
Perform medical and scientific assessment of safety data, including causality and seriousness determinations.
Support signal detection, risk assessment, and benefit-risk evaluations.
Contribute to the preparation and review of aggregate safety reports, including PBRERs, PSURs, DSURs, and annual reports.
Collaborate with Clinical Research, Regulatory Affairs, Medical Affairs, and Quality Assurance to ensure compliance with pharmacovigilance obligations.
Support health authority inspections, audits, and pharmacovigilance system assessments.
Assist in the development and maintenance of SOPs, work instructions, and pharmacovigilance processes.
Monitor compliance metrics and support continuous improvement initiatives within the safety function.
Provide training and guidance to internal stakeholders regarding pharmacovigilance requirements and reporting obligations.
Participate in vendor oversight activities for contract pharmacovigilance service providers.

Qualifications

Bachelor's degree in Nursing, Pharmacy, Public Health, Life Sciences, Medicine, or a related scientific discipline.
Minimum 5 years of pharmacovigilance, drug safety, clinical research, or related pharmaceutical industry experience.
Strong understanding of FDA, ICH, GVP, and global pharmacovigilance regulations.
Experience with adverse event case processing and safety database systems.
Excellent analytical, organizational, and communication skills.
Ability to work independently and collaboratively in a fast-paced environment.

Preferred Qualifications

MPH, MS, PharmD, MD, PA, NP, RN, or other advanced clinical/scientific degree.
Experience supporting both commercial products and clinical development programs.
Experience preparing aggregate safety reports and safety narratives.
Prior experience participating in regulatory inspections and audits.
Knowledge of signal detection and risk management activities.

Leadership Expectations (Senior Manager Level)

Lead pharmacovigilance projects and process improvement initiatives.
Serve as a subject matter expert for drug safety and regulatory compliance.
Mentor junior staff and support departmental development.
Drive operational excellence and inspection readiness.

Sunshine Act

Amphastar reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Amphastar to provide government agencies with information such as a health care provider's name, address, and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Amphastar intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Amphastar that we pay or reimburse, your name, address, and the number of payments made currently will be reported to the government.

EEO & Employment Eligibility

Amphastar is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability, or veteran status. Amphastar also complies with all applicable federal, state, and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Amphastar is an E-Verify employer.

Amphastar is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Job Type: Full-time

Pay: $110,000.00 - $140,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Health savings account
Life insurance
Paid time off
Referral program
Retirement plan

Education:

Bachelor's (Required)

Experience:

pharmacovigilance, drug safety, clinical research, or pharma: 5 years (Preferred)

Work Location: In person

Quick Apply

Refine Your Search

research scientist jobs in san dimas, ca

Pharmacovigilance Specialist

Technical Support Scientist

Administrative Program Coordinator - Adolescent and Young Adult Program

R&D Formulator

Research Scientist

Research Scientist

Senior Research Scientist

Research Associate I - Microbiome Program

Research Associate II - Cancer Biology and Molecular Medicine

R&D Gummy Formulator

Clinical Study Coordinator

Scientist II

R&D Laboratory Technician I

Research Associate - Biosensing

Clinical Trials Data Coord

Research Business Manager (Remote)

Regulatory Affairs Specialist II

Scientist and R&D Manager: Antibody Products

Research Associate II

Cognitive Scientist - AI Trainer

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