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5 дней назад

Associate Director, Global Outsourcing & Budget Management (Biotechnology)

162 000 - 180 000$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
director
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
Associate Director, Global Outsourcing & Budget Management (Biotechnology): Leading clinical outsourcing, contracting, investigator-site budgeting, supplier management, and financial reporting for global clinical studies with an accent on compliant execution, contract governance, and budget control. Focus on negotiating RFPs and clinical agreements, managing site budgets and invoices, maintaining portfolio-level financial visibility, and resolving supplier and compliance risks.

Location: Remote, with the work arrangement confirmed in the offer letter; US national and premium market compensation applies.

Annual base pay: $162,000–$180,000 for national markets; $188,000–$209,000 for premium markets including Los Angeles, San Diego, San Francisco, New York City, Chicago, and Boston. The position is also eligible for a discretionary bonus and equity award.

Company

hirify.global is a publicly traded biotechnology company developing immunotherapies, cell therapies, cancer vaccines, and treatments for infectious diseases.

What you will do

  • Lead clinical outsourcing, contracting, budgeting, and supplier-management operations across global clinical programs.
  • Plan and execute RFI/RFP activities, including scope development, bid analysis, due diligence, and supplier recommendations.
  • Negotiate and manage MSAs, work orders, statements of work, change orders, vendor agreements, and consultant agreements.
  • Develop and oversee investigator-site budgets, negotiations, payment terms, invoice reviews, audits, and billing-compliance controls.
  • Maintain portfolio-level visibility into contracts, budgets, purchase requisitions, commitments, accruals, forecasts, and variances.
  • Lead supplier-performance reviews, remediation, process improvement, audits, and cross-functional issue resolution.

Requirements

  • Bachelor’s degree in life sciences, business, finance, healthcare administration, or a related discipline; an advanced degree is preferred.
  • 8+ years of progressive experience in pharmaceutical, biotechnology, CRO, or clinical-research operations.
  • 3+ years of experience leading teams, people, or complex cross-functional workstreams.
  • Experience supporting global clinical studies across multiple phases, including RFPs, contracts, site budgets, financial tracking, and supplier performance.
  • Experience with CTMS and clinical financial, contracting, or site-payment systems; Veeva experience is strongly preferred.
  • Knowledge of Fair Market Value, coverage analysis, CPT coding, billing compliance, budgeting, forecasting, reconciliation, and variance analysis.

Nice to have

  • Advanced degree in a relevant discipline.
  • Experience with domestic and international investigator-site budget negotiations.
  • Experience with Veeva and comparable clinical systems.

Culture & Benefits

  • Collaborative environment with opportunities to work across different company functions.
  • Professional development opportunities in a growing biotechnology company.
  • Medical, dental, and vision plan options, health and financial wellness programs, and an employee assistance program.
  • Life, disability, flexible spending, retirement, education, legal, identity protection, pet insurance, and employee discount benefits.
  • Paid holidays and paid time off, including unlimited PTO for exempt employees.
  • Regular Monday–Friday schedule during standard business hours, with manager-approved flexibility.

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