ms officestakeholder managementcontract managementvendor contractsclinical operationsbudget negotiationclinical trial agreements
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$111к-166к/год
$110к$130кмедиана$150к
По похожим ролям (49) ~ $130к/год
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Роль четко очерчена: здесь есть ответственность за переговоры по клиническим контрактам и улучшение процессов. Подробные требования и условия помогают оценить предложение.
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Уровень ответственностиКлинические исследованияУдаленная работа и льготы
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Contract Manager - FSP (Clinical Trial Contracting): Reviewing, drafting, negotiating, and tracking clinical study agreements, vendor contracts, site contracts, and budgets with an accent on site contract management, study timelines, and stakeholder coordination. Focus on resolving complex contracting issues, establishing contracting processes and metrics, and guiding teams on the operational impact of contract terms.
Location: Remote, United States. Candidates must be legally authorized to work in the country of employment without employer sponsorship.
Salary: $110,700–$166,100 USD per year, plus eligibility for a discretionary annual bonus.
Company
hirify.global is the employing organization for a clinical study contract management role.
What you will do
Review, draft, negotiate, coordinate, and track confidentiality agreements, master services agreements, clinical study agreements, amendments, site contracts, consulting agreements, vendor agreements, and client contracts.
Establish and improve processes, procedures, policies, and standards for site contract management and timely contract execution.
Negotiate site budgets and advise business teams on the operational implications of contract terms.
Escalate and resolve complex issues with clients, Clinical Operations study teams, sponsors, and internal stakeholders.
Mentor and support new Senior Contract Managers and Precision staff.
Requirements
Graduate, postgraduate, or four-year college degree, or equivalent experience ideally in a scientific or healthcare discipline.
At least 7 years of relevant experience drafting, reviewing, and negotiating site Clinical Trial Agreements, vendor contracts, and site budget negotiations.
Experience leading interactions with institutions in the US, Europe, APAC, or other regions.
Experience leading interactions with Study Teams and Sponsors.
Strong organizational and written communication skills, with the ability to multitask and prioritize in a fast-paced environment.
Ability to handle time-sensitive matters accurately, exercise sound business judgment, work independently and collaboratively, and handle sensitive issues with discretion.
Professionalism, positive interpersonal skills, proactive work style, and ability to build relationships with internal and external stakeholders.
Proficiency in MS Office software and computer applications.
Nice to have
Bachelor's degree in law, a scientific field, business administration, or an equivalent discipline.
Experience setting up contracting plans and guides for CTA and budget negotiations.
Experience with Kick-Off Meetings and Bid Defense Meetings.
Experience managing relationships with study teams, CRAs, Start-up Associates, or (S)BSCAs to meet study timelines.
Culture & Benefits
Remote work in the United States within a virtual work environment.
Health insurance, retirement savings benefits, life insurance, and disability benefits.
Parental leave and paid time off for sick leave and vacation.
Work involves independent planning as well as cooperation with colleagues and customers.
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