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Pfizer
Pfizer
H1B vizos rėmėjasFarmacijos produktaiKonsultavimasRinkodara
„Pfizer“ yra pasaulinė farmacijos bendrovė, daugiausia dėmesio skirianti vaistų ir sveikatos priežiūros paslaugų, padedančių palaikyti sveikatą visą gyvenimą, kūrimui ir teikimui. Jos veikla apima mokslines inovacijas ir saugių, veiksmingų bei įperkamų gydymo būdų prieinamumo didinimą, ypatingą dėmesį skiriant vėžio ir kitų reikšmingų sveikatos sutrikimų gydymo pažangai. Bendrovės veikla gali būti aktuali specialistams, besidomintiems karjera farmacijos tyrimų, sveikatos priežiūros ir susijusių komercinių funkcijų srityse.
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Clinical Development Director, Inflammation and Immunology — Pfizer

Lead Pfizer’s clinical development programs for biologic and small molecule therapies in inflammation and immunology. Oversee study design, execution, data interpretation, and cross-functional collaboration.

USJungtinės ValstijosMAMasačusetsasPAPensilvanija
176 600 $ – 294 300 $ / metai
HibridinisVisas etatasVadovasPrivaloma Kalba: anglųDirektorius
Google Cloud Platform

Aprašymas

  • Direct development of multiple clinical studies for novel biologic and small molecule therapies across development stages
  • Lead protocol development and contribute as an individual member of clinical study teams
  • Guide study design, execution, interpretation, safety assessments, and clinically meaningful outcomes
  • Lead and support clinical development programs within project teams
  • Advise internal and external collaborators, investigators, consultants, and contractors as a technical resource
  • Contribute to publications, abstracts, presentations, and scientific communications
  • Advance clinical development strategy, study implementation, and milestones from startup through delivery
  • Lead clinical protocol preparation and contribute to consent forms, training materials, investigator brochures, analysis plans, and regulatory documents
  • Review clinical data and interpret safety and efficacy findings
  • Work with study teams to support effective study execution and completion
  • Build partnerships with Pfizer’s Biostatistics, Regulatory Affairs, Clinical Pharmacology, Clinical Operations, and other functions
  • Coordinate priorities across project teams, core study teams, and clinical sub-teams
  • Use Pfizer processes, SOPs, compliance systems, registries, and study tools to meet GCP and regulatory requirements and improve execution
  • Integrate biomarker strategies to support patient stratification, efficacy assessment, and development objectives
  • Maintain relationships with external experts, consultants, key opinion leaders, regulators, and investigator networks
  • Stay current with scientific and clinical literature in inflammation and immunology

Reikalavimai

  • PhD or PharmD with 5+ years of relevant industry experience in clinical development, clinical research, or related drug development; or MS with 7+ years; or BSc with 8+ years
  • Record of supporting development programs through key milestones
  • Strong understanding of the biopharmaceutical environment and clinical drug development
  • Familiarity with Biostatistics, Regulatory Affairs, Clinical Pharmacology, and Pharmaceutical Sciences
  • Experience developing and coaching colleagues, guiding cross-functional teams, and delivering business impact
  • Strong scientific writing, presentation, and verbal communication skills
  • Ability to build consensus, influence stakeholders, and drive change across organizational levels, including senior leadership
  • Experience reviewing clinical data listings and interpreting study data
  • Ability to conduct complex data analysis
  • Available for occasional travel of 5–10%
  • Authorized to work in the United States for any employer
  • Permanent U.S. work authorization required; visa sponsorship is not available
  • Preferred: Immunology clinical development experience
  • Preferred: Experience supporting Phase 2, Phase 3, or late-stage clinical development programs

Privalumai

  • Global Performance Plan with a bonus target of 20.0% of base salary
  • Share-based long-term incentive program
  • 401(k) plan with Pfizer matching contributions
  • Additional Pfizer retirement savings contribution
  • Paid vacation, holidays, and personal days
  • Paid caregiver, parental, and medical leave
  • Medical, prescription drug, dental, and vision coverage
  • Relocation support may be available based on business needs or eligibility

Susiję darbai

Johnson & Johnson

Director, Pharmacovigilance Alliance Contracting and Management

Johnson & Johnson
H1B vizos rėmėjasFarmacijos produktaiSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosNJNaujasis DžersisPAPensilvanija
150 000 $ – 258 750 $ / metai
HibridinisVisas etatasVadovasPrivaloma Kalba: anglųDirektorius

Lead Johnson & Johnson’s global pharmacovigilance alliance contracting team and oversee agreement strategy, negotiation, and execution. Guide partnership governance, risk and compliance, team development, and process improvement.

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Elevance Health

Clinical Programs Director, Oncology and Cardiovascular Care

Elevance Health
H1B vizos rėmėjasB2BSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosCTKonektikutasMAMasačusetsasNJNaujasis DžersisNYNiujorkasVAVirdžinija
115 200 $ – 198 720 $ / metai
HibridinisVisas etatasVadovasPrivaloma Kalba: anglųDirektorius

Lead whole-person oncology and cardiovascular programs for Elevance Health’s national accounts. Build Centers of Excellence networks and advise major healthcare clients on care solutions.

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Hiscox

Director of Technology Product Delivery

Hiscox
1 001 – 5 000 Darbuotojai
H1B vizos rėmėjasB2BDraudimasFinansai
USJungtinės ValstijosMAMasačusetsas
150 000 $ – 180 000 $ / metai
HibridinisVisas etatasVadovasPrivaloma Kalba: anglųDirektorius
AzureDebesijaKibernetinis saugumasSDLC

Lead technology delivery transformation at Hiscox USA, shifting work toward empowered product teams. Oversee delivery measurement, investment tracking, modernization, and responsible AI adoption across the software development lifecycle.

Atidaryti