Назад
Company hidden
8 дней назад

Data Science Program Lead II (Clinical Data)

109 500 - 208 500$
Формат работы
onsite
Тип работы
fulltime
Грейд
lead
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
Data Science Program Lead II (Clinical Data): Leading clinical data collection, review, quality, and database lock strategies across clinical studies with an accent on risk-based data review, clinical data science, and inspection readiness. Focus on interpreting operational data and predictive signals, managing data flows from EDC to SDTM, and aligning cross-functional stakeholders around reliable trial delivery.

Location: Irvine, California, United States

Salary: $109,500–$208,500 per year

Company

hirify.global develops medicines and healthcare solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Serve as the clinical data management subject matter expert and primary data operations contact for assigned studies.
  • Own data collection, data cleaning, data review, and database lock strategies from study start-up through study completion.
  • Lead risk-based data review, centralized monitoring, statistical review, and clinical data science activities to identify and mitigate study risks.
  • Interpret clinical and operational data, quality metrics, predictive signals, and dashboards to support study decisions, patient safety, and quality.
  • Manage data flows from raw EDC data through mapped SDTM data, triaging issues with technology teams, vendors, and service providers.
  • Lead process improvement and innovation initiatives while coaching and mentoring team members.

Requirements

  • Bachelor’s degree in business, management information systems, computer science, life sciences, or an equivalent field; a master’s degree is preferred.
  • At least 6 years of experience in pharma, clinical research, data management, or healthcare, or at least 8 years of project management experience.
  • In-depth understanding of clinical trial processes and clinical technologies.
  • Experience influencing cross-functional stakeholders without direct authority and working in a matrix environment.
  • Strong communication, analytical, coaching, and mentoring skills.
  • Knowledge of federal and applicable local regulations, Good Clinical Practices, ICH Guidelines, and quality standards.

Culture & Benefits

  • Full-time employment with paid vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) benefits for eligible employees.
  • Eligibility to participate in long-term incentive programs.
  • Equal opportunity employment with reasonable accommodation support for applicants.

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 →