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4 дня назад

Senior Clinical Site Budget Specialist (Biotechnology)

136 500 - 150 000$
Формат работы
onsite
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

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TL;DR
Senior Clinical Site Budget Specialist (Clinical Research): Developing and negotiating clinical trial site budgets, contracts, and coverage analyses with an accent on billing compliance, CMS policy, and cross-functional coordination. Focus on building study-specific budget templates, analyzing negotiation trends, managing forecasting and variance activities, and mentoring budget team members.

Location: Onsite in El Segundo, CA or Torrey Pines, CA, Monday–Friday during standard business hours; schedule flexibility is available with manager approval.

Annual base pay: $136,500–$150,000, depending on qualifications, experience, and geographic location. The position is also eligible for a discretionary bonus and equity award.

Company

hirify.global is a commercial-stage biotechnology company developing immunotherapies, cell therapies, cancer vaccines, and treatments for infectious diseases.

What you will do

  • Guide clinical operations teams through the preparation, negotiation, and execution of site budgets, service contracts, and agreements.
  • Develop and maintain study-specific budget templates, negotiation parameters, SOPs, and process-improvement recommendations.
  • Perform coverage analyses using CMS policies, NCDs, LCDs, drug compendia, and related standards.
  • Monitor budget timelines, support clinical program milestones, and provide reporting on negotiation and agreement trends.
  • Support forecasting, auditing, variance management, billing compliance, and responses to budget-related questions.
  • Partner with Legal, Finance/Accounting, and Clinical Operations while mentoring and training less-experienced budget team members.

Requirements

  • Bachelor’s degree and 7+ years of progressive experience in budget and contract development.
  • At least 4 years of experience in clinical research.
  • Advanced Excel skills and experience using Clinical Trial Management Systems, including Veeva CTMS and payments.
  • Knowledge of coverage analysis, CPT coding, the drug development process, supplier management, and billing and regulatory compliance.
  • Strong project and process management, problem-solving, communication, collaboration, and influencing skills.
  • Ability to work onsite in El Segundo or Torrey Pines, California.

Nice to have

  • Experience with contract negotiations.
  • Experience supporting domestic and international research studies.

Culture & Benefits

  • Collaborative environment with opportunities to work across different areas of the company.
  • Professional development opportunities within a growing, publicly traded biopharmaceutical company.
  • Medical, dental, and vision plan options, health and financial wellness programs, and an employee assistance program.
  • 401(k) retirement plan with company match, flexible spending accounts, disability coverage, and life insurance options.
  • Paid holidays and paid time off; exempt employees are eligible for unlimited PTO.

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