9 дней назад
Associate Director, Study Start Up (Site Budgets & Contracts)
166 000 - 200 550$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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
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.
Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →
Похожие вакансии
12 дней назад
Senior Director, New Product Strategy & Planning, North America (Biopharmaceuticals)
217 500 - 310 000$
10 дней назад
Director, Regional Market Access, Rare Diseases, Europe
119 900 - 200 400$
10 дней назад
Director, Quality Operations – Cell and Gene Therapy
215 000 - 250 000$
9 дней назад
Manager, TMF Systems and Operations (Clinical Trials)
109 200 - 174 600$
9 дней назад
Director, Regional Market Access, Rare Diseases, Europe
100 275 - 167 125$
12 дней назад
Field Reimbursement Manager (Biotech)
185 000 - 215 000$