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5 часов назад

Clinical Research Associate - Sponsor Dedicated

71 900 - 189 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle/senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Clinical Research Associate - Sponsor Dedicated (Clinical Research): Overseeing clinical trial sites across multiple therapeutic areas through site selection, initiation, monitoring, and close-out activities with an accent on protocol compliance, GCP, ICH guidelines, and patient recruitment. Focus on identifying quality issues, maintaining essential trial documentation, tracking study metrics, and coordinating with investigators, sponsors, and cross-functional project teams.

Location: Parsippany, New Jersey, United States of America; nationwide opportunities with independent on-site monitoring required.

Salary: $71,900–$189,000 annualized base pay, plus potential incentives, bonuses, and benefits.

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Conduct site selection, initiation, routine monitoring, and close-out visits across clinical studies.
  • Evaluate site performance and compliance with protocols, GCP, ICH guidelines, regulatory requirements, and sponsor expectations.
  • Support patient recruitment and retention strategies, protocol-specific training, and ongoing communication with investigative sites.
  • Track regulatory submissions, approvals, enrollment, CRF completion, data queries, and study progress.
  • Maintain complete and accurate Trial Master File and Investigator Site File documentation and prepare monitoring reports.
  • Collaborate with project teams and support study start-up, site budgets, financial management, and site payments when assigned.

Requirements

  • Bachelor’s degree in Life Sciences, Healthcare, Nursing, or a related field preferred; relevant education and experience may substitute.
  • At least 2 years of independent on-site monitoring experience in the pharmaceutical, biotechnology, or CRO industry.
  • Strong understanding of clinical research processes, GCP, ICH guidelines, and regulatory requirements.
  • Knowledge of therapeutic areas and clinical trial protocols.
  • Proficiency with Microsoft Word, Excel, PowerPoint, mobile technologies, and electronic data capture systems.
  • Strong communication, organization, problem-solving, time-management, independent-working, and collaboration skills.

Culture & Benefits

  • Full-time employment with a global healthcare and clinical development organization.
  • Opportunity to contribute to research supporting innovative medical treatments and improved patient outcomes.
  • Health and welfare benefits may be provided.
  • Incentive plans, bonuses, and other compensation may be available depending on the position.

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