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Lead Business Analyst - Sponsored Research

Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
lead
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
Lead Business Analyst - Sponsored Research (Clinical Research/Healthcare): Executing clinical trial agreements, negotiating trial budgets, configuring Clinical Trial Management Systems, and preparing Medicare Coverage Analyses with an accent on billing compliance, financial integrity, and regulatory interpretation. Focus on mentoring Sponsored Research staff, improving policies and workflows, and resolving complex research protocol and data management issues.

Location: Remote from Pennsylvania or another location within the EST or CT time zones

Company

hirify.global is a healthcare organization supporting clinical research and sponsored research operations.

What you will do

  • Lead the execution of clinical trial agreements in accordance with institutional guidelines and legal requirements.
  • Negotiate trial budgets to cover institutional administrative and clinical costs.
  • Configure clinical trial protocols and associated costs in a Clinical Trial Management System (CTMS).
  • Prepare Medicare Coverage Analyses and support compliant billing practices.
  • Mentor and train Office of Sponsored Research staff and assist with analyst performance management.
  • Develop policies, procedures, business forms, and strategic process improvements.

Requirements

  • Bachelor’s degree in business, healthcare, finance, or a related field, or six years of healthcare or clinical experience in lieu of a degree.
  • At least four years of experience in a healthcare or clinical setting.
  • Experience with clinical research, research contracting, trial budgeting and negotiations, or related research operations.
  • Hands-on experience with a CTMS and the ability to interpret clinical trial protocols for accurate data collection and compliance.
  • Knowledge of federal regulations protecting human subjects in clinical research, medical terminology, and Microsoft Word, Excel, and Teams.
  • Must be located in EST or CT time zones and able to communicate effectively, manage multiple priorities, and resolve complex research and data management issues.

Nice to have

  • Master’s degree in business, healthcare, finance, or a related field.
  • Experience as a Research Clinical Coordinator, Regulatory Specialist, Clinical Research Associate, or MCA Analyst.

Culture & Benefits

  • Work-from-home arrangement.
  • Collaborative environment involving clinical staff, researchers, and management.
  • Compliance with HIPAA, data security standards, federal and state laws, and company policies.
  • Commitment to accuracy, thoroughness, and continuous improvement.

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