
1001 - 5000 employees
Founded 2003
🏥 Healthcare
🏠Manufacturing
🧬 Biotechnology
Healthcare • Manufacturing • Biotechnology
Jazz Pharmaceuticals is a biopharmaceutical company dedicated to developing innovative medicines that address serious unmet medical needs. With a strong commitment to research and development, Jazz focuses on creating life-changing therapies, emphasizing the importance of collaboration, diversity, and employee engagement in its operations. The company prides itself on transforming patients' lives through its meaningful product offerings and a culture that fosters enthusiasm and flexibility.
đź•’ September 11
🏄 California, Pennsylvania – Remote
đź’µ $141.6k - $212.4k / year
⏰ Full Time
đźź Senior
đź‘” Manager
🦅 H1B Visa Sponsor
đź‘» Ghost score 0%
Improve your chances of getting an interview by checking your resume score before you apply.

1001 - 5000 employees
Founded 2003
🏥 Healthcare
🏠Manufacturing
🧬 Biotechnology
Healthcare • Manufacturing • Biotechnology
Jazz Pharmaceuticals is a biopharmaceutical company dedicated to developing innovative medicines that address serious unmet medical needs. With a strong commitment to research and development, Jazz focuses on creating life-changing therapies, emphasizing the importance of collaboration, diversity, and employee engagement in its operations. The company prides itself on transforming patients' lives through its meaningful product offerings and a culture that fosters enthusiasm and flexibility.
• Conduct or outsource literature searches to identify epidemiology data on disease incidence, prevalence, mortality, natural history, demographics, co-morbidities, treatment patterns and concomitant medications • Contribute epidemiology data to regulatory submissions supporting Clinical Development Programs and other processes requiring epidemiological data • Provide top of the patient funnel data for forecasting and commercial purposes • Identify appropriate US and EU secondary data sources, including administrative claims and EMR databases • Lead Requests for Proposal and Statements of Work for outsourced epidemiology studies • Support multi-disciplinary non-interventional Phase IV study teams and deliver study-related regulatory submissions • Develop statistical analysis plans with project biostatisticians • Manage external investigators, project managers and operational leads at CROs and Data Providers • Communicate with US and EU Regulatory Leads regarding submission deliverables and PMR/PMC timelines • Develop partnerships with Clinical Development, Medical Affairs, Biostatistics and Regulatory Affairs stakeholders • Communicate study plans, timelines, budgets, progress reports and study results to internal teams • Present research findings at scientific congresses and co-author peer-reviewed manuscripts • Ensure compliance with applicable laws, regulations and regulatory guidelines
• Advanced degree (MS, MPH, MSPH, or PhD) in epidemiology or a related discipline (health services research, outcomes research, public health, pharmaceutical sciences) • At least 2 years of experience in the pharmaceutical industry, CRO or in academia • Experience with rare disease studies • Project management experience in planning, budgeting, resourcing and executing the operational tasks required to complete a research study • Experience successfully coordinating cross-functional processes • Experience analyzing secondary data sources (administrative claims and EMR databases) • Excellent oral and written communication skills in English • Solid understanding of epidemiology and biostatistics • Experience managing multiple projects and reprioritizing work when necessary • Capable of working remotely with minimal supervision • Proficiency with MS Word, Excel and PowerPoint • Ability to travel approximately 10% time • Therapeutic area experience in oncology; strong knowledge of SEER data and use of SEER*Stat platform • Experience with site-based data collection in non-interventional studies (prospective patient registries and retrospective chart reviews) • Experience conducting post-marketing safety studies of marketed medicines • Experience supporting Clinical Drug Development, Safety, Forecasting and Medical Affairs teams within a biopharmaceutical company • Experience authoring protocols, study reports, and epidemiology sections of RMPs for regulatory submissions to FDA, EMA and other health authorities • Data analysis programming skills (SAS, Stata, R) or recent hands-on experience using an RWE platform technology
• Discretionary annual cash bonus or incentive compensation • Discretionary equity grants • Medical insurance • Dental insurance • Vision insurance • 401k retirement savings plan • Flexible paid vacation • Remote work arrangement
Apply Nowđź•’ September 11
Territory Business Manager driving Neogen Food Safety product sales across Minnesota, North Dakota, South Dakota, and Montana. Managing territory growth, customer relationships, prospecting, and solution-based selling.
🇺🇸 United States – Remote
⏰ Full Time
🟡 Mid-level
đźź Senior
đź‘” Manager
🦅 H1B Visa Sponsor
đź•’ September 11
Territory Business Manager driving Neogen food safety product sales across Southern Wisconsin and Northern Illinois. Managing territory growth, customer relationships, prospecting, presentations, and solution-based selling.
🇺🇸 United States – Remote
⏰ Full Time
🟡 Mid-level
đźź Senior
đź‘” Manager
🦅 H1B Visa Sponsor
đź•’ September 11
Senior supervisory principal reviewing advisor activity, accounts, and transactions at Raymond James. Providing regulatory guidance and managing risks for branches and financial advisors.
🇺🇸 United States – Remote
đź’µ $75k - $90k / year
⏰ Full Time
đźź Senior
đź‘” Manager
🦅 H1B Visa Sponsor
đź•’ September 11
Field Service Manager overseeing FiberLight’s West Texas fiber installations, maintenance, construction, and restoration. Managing contractors, permitting, field teams, materials, estimates, and network planning.
🇺🇸 United States – Remote
đź’° $500M Debt Financing - FiberLight on 2025-04
⏰ Full Time
🟡 Mid-level
đźź Senior
đź‘” Manager
đź•’ September 11
Senior Manager advancing fatherhood and family programs across Care Net’s pregnancy-center network. Creating resources, leading events, and mentoring fatherhood practitioners.