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6 дней назад

Sr. Study Operations Specialist (Oncology)

Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
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
Sr. Study Operations Specialist (Oncology) (Clinical Research/Oncology): Coordinating and supporting oncology clinical studies from planning and enrollment through follow-up and close-out with an accent on protocol compliance, patient prescreening, and accurate study data. Focus on reviewing medical records, collaborating with investigators and research teams, and improving clinical study operations through quality management and process optimization.

Location: Remote within the United States

Company

hirify.global supports community oncologists through a patient-centric, physician-driven, and technology-powered healthcare model focused on improving outcomes for people living with cancer and other diseases.

What you will do

  • Support the planning, implementation, management, enrollment, follow-up, and close-out of oncology clinical studies.
  • Coordinate patient recruitment and prescreening across the network portfolio by reviewing medical records and identifying eligible participants.
  • Document patient information and screening outcomes accurately in EMR and clinical trial management systems.
  • Collaborate with healthcare providers, study coordinators, principal investigators, clinicians, research staff, sponsors, CROs, and regulatory authorities.
  • Ensure study data is accurate, complete, and consistent while maintaining compliance with protocols and regulatory requirements.
  • Identify and implement process improvements and best practices to improve study quality and operational efficiency.

Requirements

  • At least 5 years of experience in clinical research, clinical study coordination, or oncology nursing preferred.
  • Bachelor’s degree in nursing, life sciences, or a related field; an advanced degree such as a Master’s, RN, or NP is preferred, or equivalent experience.
  • Knowledge of GCP, ICH guidelines, and applicable regulatory requirements.
  • Experience leading quality management initiatives, audits, inspections, and process improvements.
  • Strong analytical, organizational, project management, communication, and interpersonal skills.
  • Experience with EDC systems, CTMS, and other clinical research technologies is preferred.

Culture & Benefits

  • Values-driven culture with startup enthusiasm supported by leaders in oncology, urology, technology, and finance.
  • Cross-functional collaboration with clinicians, research staff, regulatory affairs personnel, and subject matter experts.
  • Opportunity to improve processes that support independent physicians and the patients they serve.
  • Full-time remote work arrangement within the United States.

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