Top 187 associate director, document control Jobs in menlo park, 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
Associate Medical Director, Medical Safety
Jazz Pharmaceuticals —Palo Alto, CA
- $212,000 - $318,000 a year
- Medicine
- Computer literacy
- 3 years
- 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
Associate Director, Medical Safety (Scientist)
Jazz Pharmaceuticals —California
- $156,000 - $234,000 a year
- Bachelor of Science
- Windows
- Presentation skills
- Health insurance
- Dental insurance
Controlled Document Management System (CDMS) Administrator and Document Specialist
SLAC National Accelerator Laboratory —Menlo Park, CA
- $119,613 - $170,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Office
Associate Director, Document Control
Corcept Therapeutics —Redwood City, CA
- $186,500 - $219,400 a year
- Hybrid work
- Bachelor of Science
- Office
- Mentoring
Associate Director of Meetings and Special Events
Marriott International, Inc —Half Moon Bay, CA
- $104,000 - $138,000 a year
- Full-time
- Research
- Mid-level
- Hotel
Associate Athletics Director - Student-Athlete Success & Performance
Menlo School —Atherton, CA
- $150,000 - $190,000 a year
- Weekends as needed
- Google Workspace
- Doctoral degree
- 5 years
- Retirement plan
Associate Director, Customer Success (Commerce & Retail Media)
PubMatic —Redwood City, CA
- $180,000 - $220,000 a year
- Urgently hiring
- Hybrid work
- 5 years
- Office
- Bachelor's degree
- Commuter assistance
- Paid holidays
Quick Apply
Associate Director, Supply Chain (Logistics)
Corcept Therapeutics —Redwood City, CA
- $180,900 - $212,800 a year
- Hybrid work
- Office
- 8 years
- Bachelor's degree
Quick Apply
Associate Director, Editorial & Operations
San Francisco Bay University —Fremont, CA
- $100,000 - $150,000 a year
- Weekends as needed
- Hybrid work
- 6 years
- Marketing
- Office
Quick Apply
Sr Mgr/Associate Director, Global Consolidations, Reporting & Systems
Guardant Health —Palo Alto, CA
- $139,230 - $225,250 a year
- Email
- Hybrid work
- Background check
- Oracle
- CPA
Associate Director, Supply Chain (Commercial)
Corcept Therapeutics —Redwood City, CA
- $180,900 - $212,800 a year
- Hybrid work
- Microsoft Excel
- Office
- 8 years
Quick Apply
Senior Manager / Associate Director, Healthcare Compliance
Orca Bio —Menlo Park, CA
- $160,000 - $200,000 a year
- Full-time
- Remote
- 6 years
- Bachelor's degree
- Travel
- Disability insurance
- Health insurance
Project Coordinator
JE Dunn —Santa Clara, CA
- $65,851 - $82,313 a year
- Email
- Background check
- Mid-level
- Office
Associate Director/ Director, Supply Chain Management
Synthekine —Menlo Park, CA
- $180,000 - $240,000 a year
- Bachelor of Science
- Office
- Project management
- Commuter assistance
- Health savings account
ASSOCIATE DIRECTOR, ACCOUNTING MANAGER
Cresset Capital —Palo Alto, CA
- $140,000 - $165,000 a year
- Microsoft Word
- 7 years
- Customer service
- Health savings account
- Disability insurance
Quick Apply
Configuration Data Management Analyst Staff
Lockheed Martin Corporation —Sunnyvale, CA
- $90,200 - $159,045 a year
- Full-time
- Microsoft Access
- Writing skills
- Mid-level
- Paid jury duty
- Paid holidays
2d
Associate Director, Clinical Science
Natera —San Carlos, CA
- $174,700 - $218,400 a year
- Remote
- Medicine
- Computer literacy
- HIPAA
- Commuter assistance
- Health 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

associate director, document control jobs in menlo park, ca

Associate Director, Medical Safety (Scientist)

Associate Director, Medical Safety (Scientist)

Associate Medical Director, Medical Safety

Associate Director, Medical Safety (Scientist)

Associate Director, Medical Safety (Scientist)

Controlled Document Management System (CDMS) Administrator and Document Specialist

Associate Director, Document Control

Associate Director of Meetings and Special Events

Associate Athletics Director - Student-Athlete Success & Performance

Associate Director, Customer Success (Commerce & Retail Media)

Associate Director, Supply Chain (Logistics)

Associate Director, Editorial & Operations

Sr Mgr/Associate Director, Global Consolidations, Reporting & Systems

Associate Director, Supply Chain (Commercial)

Senior Manager / Associate Director, Healthcare Compliance

Project Coordinator

Associate Director/ Director, Supply Chain Management

ASSOCIATE DIRECTOR, ACCOUNTING MANAGER

Configuration Data Management Analyst Staff

Associate Director, Clinical Science

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