Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
Пожаловаться
Зарплата и рынок
ЗП не указана
На похожих ролях по рынку
$94к$126кмедиана$178к
50 в выборке
76
Хорошая вакансия
развернуть
Обязанности понятны и связаны с клиническими исследованиями в крупной CRO-компании, но без указанной зарплаты сложно оценить условия относительно рынка.
Кликните для подробной информации
Зарплата не указанаЧёткие обязанностиСфера медицины
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Подключить Plus
Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Contract Negotiation Specialist (North America Team) (Clinical Research/Contract Negotiation): Managing the preparation, review, and negotiation of clinical site agreements for study start-up activities with an accent on contract execution, budget alignment, and regulatory compliance. Focus on resolving contract delays, coordinating with cross-functional stakeholders, and maintaining accurate documentation for audit readiness.
Location: Home-based role in São Paulo, Brazil; Buenos Aires, Argentina is also listed as an available location.
Company
IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
Draft, review, and negotiate clinical trial agreements, confidentiality agreements, amendments, and related site contracts.
Manage an assigned contract portfolio supporting site activation deliverables and study timelines.
Coordinate contract-related matters with investigative sites and internal teams, including Site Activation, Clinical Operations, Finance, and Legal.
Apply approved negotiation parameters, escalate non-standard or higher-risk terms, and resolve contract-related delays.
Track contract progress, maintain accurate documentation, and provide status updates and metrics.
Support regulatory compliance, audit readiness, and continuous improvements to contract cycle times and quality.
Requirements
Bachelor’s degree.
At least two years of clinical research experience in a CRO or pharmaceutical company.
Direct experience with contract and budget negotiation with clinical sites.
Advanced English skills are required for supporting sites in North America.
Ability to manage multiple priorities while meeting established timelines and quality expectations.
Culture & Benefits
Home-based work arrangement.
Collaboration with cross-functional clinical research and study start-up teams.
Work supporting clinical studies and the development of medical treatments.
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 →