Назад
Company hidden
обновлено 6 дней назад

Site Contracts Associate (Clinical Research)

49 200 - 123 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior
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
Site Contracts Associate (Clinical Research): Developing investigator grant estimates and managing site contracting activities for clinical trials with an accent on contract budgets, operational support, and regulatory compliance. Focus on maintaining contract systems and templates, coordinating with sponsors and regional teams, and monitoring contracting timelines and financial goals.

Location: Durham, North Carolina, United States of America

Annual base pay: $49,200.00–$123,000.00

Company

hirify.global Biotech is a full-service contract research organization serving biotech sponsors with clinical research, healthcare intelligence, and life sciences services.

What you will do

  • Develop investigator grant estimates and proposal text for business development and proposal creation.
  • Maintain contract and budget templates, systems, tools, and training materials for assigned sponsors, studies, and programs.
  • Collaborate with sponsors, internal stakeholders, and regional and country teams to deliver project scope and meet sponsor requirements.
  • Provide operational and financial contracting support for clinical trial initiation and maintenance while ensuring regulatory compliance.
  • Prepare and review scientific, technical, and administrative documentation supporting study start-up and ongoing trial activities.
  • Monitor contracting efficiency, timelines, financial goals, performance metrics, out-of-scope activities, records, and quality standards.

Requirements

  • 1–3 years of experience negotiating clinical site contracts and budget templates.
  • Strong understanding of clinical research processes and regulatory requirements.
  • Proficiency in Microsoft Office and contract management systems.
  • Excellent organizational, analytical, and communication skills.

Nice to have

  • Bachelor’s degree in business, life sciences, or a related field.
  • Experience in clinical trial budgeting, contracting, or site management.

Culture & Benefits

  • Equal opportunity employment environment.
  • Health and welfare benefits may be offered.
  • Incentive plans, bonuses, and other compensation may be available depending on the position.

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 →