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9 дней назад

Associate Director, Study Start Up (Site Budgets & Contracts)

166 000 - 200 550$
Формат работы
onsite
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, Study Start Up (Site Budgets & Contracts) (Oncology Clinical Operations): Building and governing procedure-level site budgets and clinical trial agreements for global oncology studies with an accent on Fair Market Value, country-specific cost structures, and rapid contract execution. Focus on negotiating investigator site budgets, coordinating Legal and Finance requirements, managing CRO vendors, and improving cycle-time performance for site activation.

Location: Jersey City, NJ; onsite presence required at least 3 days per week

Salary: $166,000–$200,550 per year, depending on skills, competency, and market demand.

Company

hirify.global Therapeutics is a biopharmaceutical company developing novel treatments using technology that combines chemistry, engineering, computation, and biology.

What you will do

  • Own global and country-specific investigator site budget development across assigned oncology studies.
  • Translate clinical protocols into procedure-level budgets, incorporating oncology cost drivers such as biopsies, biomarker assessments, imaging, patient stipends, and drug handling.
  • Lead site budget and payment-term negotiations, including escalation of requests outside approved parameters.
  • Coordinate clinical trial agreement and budget finalization with Legal, Finance, Clinical Data Management, vendors, and investigator payment teams.
  • Track budget and contract cycle-time KPIs, forecast site activation timelines, and lead process improvements.
  • Oversee CRO and outsourced contracting vendors while coaching and developing study start-up and site-contracting staff.

Requirements

  • 10+ years of relevant experience with a bachelor's degree, or 8+ years with a postgraduate degree, including extensive clinical operations, study start-up, or investigator site budget experience.
  • Expertise building site budgets from protocols using procedure-level benchmarking tools such as IQVIA GrantPlan, CPT and procedure-code mapping, country-specific cost structures, and Fair Market Value principles.
  • Strong knowledge of clinical trial start-up processes and experience managing multiple clinical trials.
  • Strong familiarity with Veeva Vault Clinical, including CTMS and eTMF.
  • Excellent project management, communication, organization, and stakeholder relationship skills.
  • Oncology trial experience, US coverage analysis or Medicare Coverage Analysis, global CTA and budget templates, or relevant professional certification are preferred.

Culture & Benefits

  • Onsite collaboration and operational support in Jersey City at least three days per week.
  • Annual bonus and equity compensation.
  • 401(k) plan with company matching.
  • Medical, dental, vision, mental health, wellness, life, and AD&D insurance benefits.
  • Paid time off, holiday policies, enhanced parental leave, and summer and winter holiday shutdowns.
  • Daily subsidized lunch when working onsite.

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