Назад
Company hidden
8 дней назад

Scientist, Trial Support (Pharmacokinetics)

Формат работы
remote (только USA)/hybrid
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Scientist, Trial Support (Pharmacokinetics): Supporting PK/PD research and clinical study data deliveries through sample management, bioanalytical reporting, and LIMS administration with an accent on clinical and nonclinical study operations, data integrity, and cross-functional coordination. Focus on defining studies in LIMS, managing clinical samples, reviewing technical documents, and tracking data-cleaning activities across multiple studies and service providers.

Location: Spring House, Pennsylvania, United States of America. Hybrid work is indicated, with remote work options considered on a case-by-case basis if approved by the company.

Company

Johnson & Johnson develops healthcare, Innovative Medicine, and MedTech solutions across the spectrum of disease prevention, treatment, and care.

What you will do

  • Support pharmacokinetic/pharmacodynamic research projects and drug development programs.
  • Coordinate clinical and nonclinical study deliveries, sample management, and bioanalytical data reporting.
  • Partner with clinical operations, bioanalytical groups, compliance, central laboratories, clinical trial teams, and external providers.
  • Review protocols, statements of work, lab manuals, and other study specifications.
  • Define studies in LIMS, manage sample inventories, and support sample acquisition, storage, and disposition.
  • Generate status reports, contribute to process and system optimization, and coach junior colleagues.

Requirements

  • Bachelor’s degree with 3 years of relevant experience, master’s degree with 2 years, or PhD with 1 year of relevant experience.
  • Experience in sample management and database systems such as Watson LIMS or LabVantage LIMS.
  • Experience reviewing laboratory technical documents, including protocols, statements of work, and lab manuals.
  • Experience in GLP/GCP environments.
  • Strong communication, organization, attention to detail, and time-management skills.

Nice to have

  • Experience with clinical data management, clinical pharmacology, pharmacometric modeling, study management, scientific research, and regulatory environments.
  • Coaching experience and strong analytical or report-writing skills.

Culture & Benefits

  • Work within multidisciplinary teams supporting medicines from discovery through post-market clinical development.
  • Contribute to patient-focused healthcare innovation across Innovative Medicine and MedTech.
  • Inclusive work environment focused on individual dignity, diversity, and equal opportunity.
  • Remote work may be available on a case-by-case basis with company approval.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →