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1 день назад

Senior Contract Manager - FSP

110 700 - 166 100$
Формат работы
remote (только USA)
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

Текст:
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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.
  • Track contract metrics, execution status, expirations, obligations, files, databases, and archives.
  • 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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