Top 60 associate scientist Jobs in malvern pa

Associate Director, Medical Safety (Scientist)
Jazz Pharmaceuticals —Philadelphia, PA
- $156,000 - $234,000 a year
- Bachelor of Science
- Windows
- Presentation skills
- Health insurance
- Dental insurance
Associate Director, Medical Safety (Scientist)
Jazz Pharmaceuticals —Philadelphia, PA
- $156,000 - $234,000 a year
- Bachelor of Science
- Windows
- Presentation skills
- Health insurance
- Dental insurance
Blood Bank Technologist
Main Line Health —Paoli, PA
- 8 hour shift
- Hospital
- Mid-level
- Experience equivalent to degree accepted
- Free parking
- 403(b) matching
Associate Scientist
Frontage Laboratories —Exton, PA
- Full-time
- Research
- Mid-level
- Master's degree
- Disability insurance
- Health insurance
Quick Apply
Associate Scientist/Scientist-Biologics
Frontage Laboratories —Exton, PA
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
Associate Scientist-Biologics
Frontage Laboratories —Exton, PA
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
Scientist/Associate Scientist- Biomarker
Frontage Laboratories —Exton, PA
- Full-time
- Bachelor of Science
- Research
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
Associate Scientist, Pharmaceutical Analysis, Small Molecule
Frontage Laboratories —Exton, PA
- Full-time
- Bachelor of Science
- Bachelor's degree
- Entry level
- Disability insurance
- Health insurance
Quick Apply
Associate Scientist, Bioanalytical Services
Frontage Laboratories —Exton, PA
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
Senior Associate Chemist (Environmental Consulting, Seller-Doer)
Onterris —Valley Forge, PA
- $120,000 - $150,000 a year
- Full-time
- Bachelor's degree
- Travel
- Senior level
Research Associate, In Vivo Analytical Development
Kite Pharma —Philadelphia, PA
- $74,715 - $96,690 a year
- Full-time
- High school diploma or GED
- Associate's degree
- Communication skills
- Health insurance
- Dental insurance
Scientist I, Study Administrator
Franklin Bio Lab —King of Prussia, PA
- Weekends as needed
- Microsoft Outlook
- Current TB test
- Writing skills
- Health savings account
- AD&D insurance
Quick Apply
6d
Environmental Scientist/Engineer
Edward B. Walsh & Associates —Exton, PA
- Email
- Mid-level
- Communication skills
Senior Associate Chemist (Environmental Consulting, Seller-Doer)
Environmental Standards, Inc. —Valley Forge, PA
- $120,000 - $150,000 a year
- Full-time
- Bachelor's degree
- Travel
- Senior level
Associate QC Specialist
Frontage Laboratories —Exton, PA
- Full-time
- Microsoft Word
- Mid-level
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
Clinical Laboratory Scientist
Main Line Health —Wynnewood, PA
- Part-time
- Hospital
- Organizational skills
- Computer skills
- Free parking
- Tuition reimbursement
Research Technician II- Cellular and Molecular Therapeutics
Children’s Hospital of Philadelphia —Philadelphia, PA
- $43,900 - $53,440 a year
- Full-time
- High school diploma or GED
- Analysis skills
- Neurology
Quick Apply
Staff Geologist / Scientist I
Roux Associates, Inc. —Logan Township, NJ
- $65,000 - $75,000 a year
- Extended hours
- Hybrid work
- Construction site
- Office
- Analysis skills
- Profit sharing
- Paid parental leave
Research Associate, Cell Biology
Kite Pharma —Philadelphia, PA
- $74,715 - $96,690 a year
- Full-time
- High school diploma or GED
- Bachelor's degree
- Organizational skills
- Health insurance
- Dental insurance
5h
Associate Scientist
LANXESS Corporation —Wilmington, DE
- Full-time
- Mid-level
- Databases
- Bachelor's degree
- Health insurance
- Retirement plan
6d

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Associate Director, Medical Safety (Scientist)

Jazz Pharmaceuticals -
Philadelphia, PA

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 scientist jobs in malvern pa

Associate Director, Medical Safety (Scientist)

Associate Director, Medical Safety (Scientist)

Blood Bank Technologist

Associate Scientist

Associate Scientist/Scientist-Biologics

Associate Scientist-Biologics

Scientist/Associate Scientist- Biomarker

Associate Scientist, Pharmaceutical Analysis, Small Molecule

Associate Scientist, Bioanalytical Services

Senior Associate Chemist (Environmental Consulting, Seller-Doer)

Research Associate, In Vivo Analytical Development

Scientist I, Study Administrator

Environmental Scientist/Engineer

Senior Associate Chemist (Environmental Consulting, Seller-Doer)

Associate QC Specialist

Clinical Laboratory Scientist

Research Technician II- Cellular and Molecular Therapeutics

Staff Geologist / Scientist I

Research Associate, Cell Biology

Associate Scientist

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