Top 233 Research associate Jobs in Foster City Ca

Associate Director, Medical Safety (Scientist)
Jazz Pharmaceuticals —Palo Alto, CA
- $156,000 - $234,000 a year
- Bachelor of Science
- Windows
- Presentation skills
- Health insurance
- Dental insurance
Associate Director, Medical Safety (Scientist)
Jazz Pharmaceuticals —Palo Alto, CA
- $156,000 - $234,000 a year
- Bachelor of Science
- Windows
- Presentation skills
- Health insurance
- Dental insurance
Senior/Principal Research Associate Cancer Biology
Beacon Hill Life Sciences —South San Francisco, CA
- From $60 an hour
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Free parking
- Health insurance
Quick Apply
Senior Research Associate, Cancer Biology (CrispR)
Yoh, A Day & Zimmermann Company —San Francisco, CA
- $55 - $70 an hour
- Bachelor of Science
- 3 years
- Bachelor's degree
- Health savings account
- Disability insurance
Quick Apply
Conflicts Research Assistant
Legal Specialists —San Francisco, CA
- $57,000 - $74,500 a year
- Weekends as needed
- Hybrid work
- Writing skills
- Mid-level
- Office
Quick Apply
14h
Associate Director, Medical Safety (Scientist)
Jazz Pharmaceuticals —California
- $156,000 - $234,000 a year
- Bachelor of Science
- Windows
- Presentation skills
- Health insurance
- Dental insurance
Associate Director, Medical Safety (Scientist)
Jazz Pharmaceuticals —California
- $156,000 - $234,000 a year
- Bachelor of Science
- Windows
- Presentation skills
- Health insurance
- Dental insurance
Experienced Clinical Research Associate - Full-Service
Syneos - Clinical and Corporate - Prod —California
- $70,100 - $126,100 a year
- Full-time
- Mid-level
- Bachelor's degree
- Team management
- Employee stock purchase plan
- Health insurance
3d
Research Associate - pharma
MEDVACON —Foster City, CA
- Contract
- Microsoft Word
- Microsoft Excel
- Customer service
Quick Apply
Research Associate, Analytical Ops
Gilead Sciences —Foster City, CA
- $82,195 - $106,370 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
Senior Research Associate, FPD
Gilead Sciences —Foster City, CA
- $94,945 - $122,870 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
Neuroimaging Research Assistant
Stanford University —Stanford, CA
- $38.55 - $46.68 an hour
- Extended hours
- English
- Mid-level
- Databases
Senior Research Associate
Natera —San Carlos, CA
- $87,300 - $109,100 a year
- Bachelor of Science
- Mid-level
- 3 years
- Commuter assistance
- Health insurance
Research Associate 1
Natera —San Carlos, CA
- $25 - $30 an hour
- Full-time
- Bachelor of Science
- HIPAA
- Office
- Commuter assistance
- Disability insurance
7d
Research Associate II
BridgeBio Pharma —San Carlos, CA
- $94,800 - $105,200 a year
- Hybrid work
- Mid-level
- Master's degree
- Bachelor's degree
- Commuter assistance
- Paid parental leave
Research Associate I/II, Production
BigHat Biosciences —San Mateo, CA
- $75,000 - $105,000 a year
- Full-time
- Google Workspace
- Bachelor of Science
- Research
- Paid parental leave
- Paid holidays
Quick Apply
Project Associate, Research
Gilead Sciences —Foster City, CA
- $117,895 - $152,570 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- High school
- Health insurance
- Dental insurance
1d
Associate Scientist, FPD
Gilead Sciences —Foster City, CA
- $109,650 - $141,900 a year
- Full-time
- Bachelor of Science
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Research Associate / Senior Research Associate, Development Chemistry
Eyconis —Redwood City, CA
- $78,000 - $90,000 a year
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
Quick Apply
Associate Scientist, Protein Engineering & Binder Optimization
Kite Pharma —Foster City, CA
- $109,650 - $141,900 a year
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance

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Associate Director, Medical Safety (Scientist)

Jazz Pharmaceuticals -
Palo Alto, CA

Apply Now

Job Details

$156,000 - $234,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Vision insurance

Qualifications

Medical writing
Pharmacovigilance research
Safety regulations
Database searching for reference services
Windows
Computer skills
Literature search services
Clinical program risk management
Cross-functional collaboration
Patient safety and incident reporting systems
Cross-functional team management
Medical terminology
Cross-functional communication

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.

The Associate Director, Medical Safety (Scientist) is a key member of the Medical Safety team. This role is responsible for ensuring up to date processes / procedures for safety governance, signal management, clinical surveillance, periodic safety reporting, and risk management and/or driving innovation initiatives within Medical Safety organization. In close collaboration with Medical Safety Physician and/or Medical Safety Scientist line manager, this role is also responsible for contributing to regulatory submission safety strategy. Other responsibilities include but are not limited to: signal management activities, production of aggregate safety reports (e.g., DSURs, PADERs, PBRERs), provision of high-level scientific expertise in the safety evaluation and risk management strategies of assigned products (e.g, signal evaluation reports, health hazard evaluations, and RMPs), global leadership / representation of Medical Safety within the company (e.g., leading Safety Management Teams, presenting at Executive Safety Board meetings), and SME support for HA inspections.

Essential Functions

Leads cross-functional safety management teams (SMTs) and drives safety strategy for responsible product/program.
Ensures that processes and procedures are up to date to meet regulatory requirements and inspection readiness
Drives signal management process using available methodologies, including making recommendations for the assessment and prioritization of safety concerns.
Effectively communicates with members of the interdisciplinary team regarding ongoing signal evaluation.
Ensures that available safety information is evaluated in order to meet both internal and external requirements, including identifying the need for labeling updates. Produces accurate and fit for purpose evaluation documents with clear conclusions, as required.
Leads the coordination of aggregate safety reports (PBRERs, DSURs, PADERs) and authors relevant sections, as appropriate.
Authors or provides guidance for the production of risk management plans (RMPs).
Provides strategic input into regulatory requests / responses.
Delivers clinical safety input into clinical development program.
Leads the medical safety contributions of global regulatory submissions for new products, formulations or indications.
Participates in and/or leads internal safety surveillance meetings as well as joint safety meetings with licensing partners, as needed.
Provides medical safety input into creation / review of Safety Data Exchange Agreements and/or other PV agreements.
Escalates issues / concerns to senior management in a timely and appropriate manner.
Mentors and trains junior members of the Medical Safety team.

Required Knowledge, Skills, and Abilities

Minimum Requirements

At least 6 years of experience in drug safety, including at least 4 years of experience in surveillance / risk management.
Ability to independently search clinical safety and literature databases for relevant information.
Expert knowledge of pharmacovigilance regulations regarding aggregate safety reports, risk management plans, and signal management.
Excellent medical writing skills, as well as proven ability to effectively lead interdisciplinary teams.
In-depth knowledge of medical and drug terminology, as well as the clinical development process.
Familiarity with MedDRA and safety databases; Proficient with Windows applications, and ability to learn new programs / databases.

Required/Preferred Education and Licenses

Requires a degree (e.g., BS, BA, MSc or PhD) or professional qualification in a life science field (e.g., nursing or pharmacy) or a relevant scientific/technical discipline and experience.

#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: $156,000.00 - $234,000.00

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

research associate jobs in foster city ca

Associate Director, Medical Safety (Scientist)

Associate Director, Medical Safety (Scientist)

Senior/Principal Research Associate Cancer Biology

Senior Research Associate, Cancer Biology (CrispR)

Conflicts Research Assistant

Associate Director, Medical Safety (Scientist)

Associate Director, Medical Safety (Scientist)

Experienced Clinical Research Associate - Full-Service

Research Associate - pharma

Research Associate, Analytical Ops

Senior Research Associate, FPD

Neuroimaging Research Assistant

Senior Research Associate

Research Associate 1

Research Associate II

Research Associate I/II, Production

Project Associate, Research

Associate Scientist, FPD

Research Associate / Senior Research Associate, Development Chemistry

Associate Scientist, Protein Engineering & Binder Optimization

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