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6 дней назад

CRA 2, Oncology, IQVIA Biotech (Oncology)

74 500 - 175 100$
Формат работы
onsite
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:
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TL;DR
CRA 2, Oncology, IQVIA Biotech (Oncology): Monitoring and managing clinical trial sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations with an accent on oncology solid tumor studies, site performance, and data integrity. Focus on conducting site visits, tracking recruitment and regulatory submissions, maintaining TMF and ISF documentation, and resolving site-level quality issues.

Location: Durham, North Carolina, United States of America; travel required as needed by the project.

Salary: $74,500–$175,100 annualized base pay, with actual compensation varying by qualifications, location, and schedule.

Company

hirify.global Biotech is a full-service clinical research organization serving biotech sponsors with therapeutically aligned clinical development solutions.

What you will do

  • Conduct site selection, initiation, monitoring, and close-out visits in line with the contracted scope of work, GCP, and ICH guidelines.
  • Collaborate with site staff on subject recruitment strategies, enrollment goals, and project timelines.
  • Deliver protocol and study-specific training and maintain communication with site personnel.
  • Assess site performance, protocol adherence, data integrity, and quality concerns.
  • Track regulatory submissions, enrollment, CRF completion, data queries, and essential documents in the TMF and ISF.
  • Document visit outcomes and support recruitment planning, invoice collection, budget tracking, and cross-functional study execution.

Requirements

  • Bachelor’s degree in life sciences or a health-related field, or equivalent experience.
  • At least 1 year of on-site monitoring experience.
  • Experience monitoring oncology solid tumor studies.
  • Strong understanding of GCP, ICH guidelines, and regulatory requirements.
  • Ability to travel as required by the project.

Culture & Benefits

  • Work within a clinical monitoring team supporting biotech sponsors.
  • Contribute to the quality and integrity of clinical research data.
  • Health and welfare benefits may be available depending on the position offered.
  • Additional incentive plans, bonuses, or other compensation may be offered depending on the position.

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