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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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Darbai įmonėje

Clinical Development Director, Inflammation and Immunology

Lead Pfizer’s clinical development programs and trials for biologic and small-molecule therapies in inflammation and immunology. Guide study design, data review, cross-functional delivery, and regulatory compliance.

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

Aprašymas

  • Direct development of multiple clinical studies for novel biologic and small-molecule therapies across development stages.
  • Lead clinical protocol development and contribute as an individual member of clinical study teams.
  • Set scientific direction for study design, execution, interpretation, safety assessment, and clinically meaningful outcomes.
  • Lead and support clinical development programs within project teams.
  • Provide technical guidance to internal and external collaborators, investigators, consultants, and contractors.
  • Contribute to publications, abstracts, presentations, and other scientific communications.
  • Support clinical development strategy, study implementation, and milestones from startup through conduct and delivery.
  • Lead clinical protocol preparation and contribute to consent forms, training materials, investigator brochures, statistical analysis plans, and regulatory documents.
  • Oversee clinical data review, including the collection, analysis, and interpretation of safety and efficacy results.
  • Work with study teams to support effective execution and completion.
  • Build partnerships across Pfizer functions, including Biostatistics, Regulatory Affairs, Clinical Pharmacology, and Clinical Operations.
  • Coordinate priorities across project teams, core study teams, and clinical sub-teams.
  • Maintain compliance with Good Clinical Practice, regulatory requirements, Institutional Review Boards, and Pfizer standards.
  • Use Pfizer compliance platforms, registries, and study systems to strengthen study execution.
  • Integrate biomarker strategies into therapeutic area programs.
  • Build and maintain relationships with external experts, consultants, key opinion leaders, regulators, and investigator networks.
  • Stay current with scientific and clinical literature relevant to inflammation and immunology.

Reikalavimai

  • PhD or PharmD and at least 5 years of relevant industry experience in clinical development, clinical research, or related drug development, with a record of advancing programs through key milestones; or an MS and at least 7 years of relevant experience; or a bachelor's degree and at least 8 years of relevant experience.
  • In-depth knowledge of the biopharmaceutical sector 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 meaningful business impact.
  • Strong scientific writing, presentation, and verbal communication skills.
  • Ability to build consensus, influence stakeholders, and lead change across organizational levels, including senior leadership.
  • Substantial 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 is required.
  • U.S. work visa sponsorship is not available now or in the future.

Privalumai

  • Target bonus equal to 20% of base salary through Pfizer’s Global Performance Plan.
  • Eligibility for Pfizer’s 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.
  • Relocation assistance may be available depending on business needs and 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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H1B vizos rėmėjasB2BSveikatos draudimasSveikatos priežiūra
USJungtinės ValstijosCTKonektikutasMAMasačusetsasNJNaujasis DžersisNYNiujorkasVAVirdžinija
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HibridinisVisas etatasVadovasPrivaloma Kalba: anglųDirektorius

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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.

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