Назад
Company hidden
1 день назад

Senior Clinical Trial Associate (Oncology)

110 000 - 115 000$
Тип работы
fulltime
Грейд
senior
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
Senior Clinical Trial Associate (Oncology): Supporting the execution of in-house and outsourced oncology clinical trials with an accent on study documentation, vendor coordination, investigator-site communication, and Trial Master File quality. Focus on overseeing sample logistics, reconciling study processes, managing operational risks, and coordinating contracts, budgets, invoices, and payments.

Location: Based out of the San Francisco or Cambridge office; approximately 10% travel required

Salary: $110,000–$115,000 annually, plus equity, bonus, and benefits.

Company

hirify.global is a clinical-stage biopharmaceutical company developing therapies for breast cancer, including palazestrant and OP-3136.

What you will do

  • Provide administrative and operational support to Clinical Trial Leads and Study Execution Teams across study start-up, maintenance, and closeout.
  • Coordinate clinical trial activities with internal teams, investigator sites, CROs, contract laboratories, and other vendors.
  • Manage study documentation, correspondence, materials, trackers, financial records, and Trial Master File activities.
  • Oversee sample collection, shipment, and analysis, while reconciling study processes and escalating issues.
  • Support vendor management plans, study metrics, contracts, budgets, invoices, payments, central IRB submissions, and site-specific informed consent forms.
  • Contribute to Clinical Operations initiatives, SOPs, quality control reviews, meeting coordination, and departmental administration.

Requirements

  • Bachelor’s degree.
  • At least 3 years of related industry experience, including 2 years working as a Clinical Trial Associate.
  • Working knowledge of clinical protocols and proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.
  • Experience leading small-group meetings and/or managing vendor relationships.
  • Strong organization, attention to detail, teamwork, collaboration, and written and verbal communication skills.
  • Ability to accommodate a flexible work schedule according to clinical trial priorities.

Nice to have

  • Familiarity with FDA and EMA regulatory requirements and ICH/GCP guidelines.

Culture & Benefits

  • Competitive compensation and benefits package.
  • Equity and bonus opportunities.
  • Open, flexible, and friendly work environment.
  • Support for long-term career development.
  • Culture focused on excellence, adaptability, collaboration, and improving patient outcomes.

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 →