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7 дней назад

IQVIA Biotech - Global Site Activation, Senior Manager, Legal Council

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
Bulgaria
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
IQVIA Biotech - Global Site Activation, Senior Manager, Legal Council (Clinical Trial Contracting): Providing operational legal support for clinical trial contracting, including contract templates, country-specific guidance, and issue resolution with an accent on regulated clinical research and cross-functional governance. Focus on maintaining global site contract libraries, standardizing contracting practices, training site contract teams, and applying GCP/ICH requirements.

Location: Sofia, Bulgaria

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Provide study-specific contracting support to Project Managers, SSUMs, Site Contract Negotiators, and Global Template Developers.
  • Resolve complex contracting issues, advise on approved contracting positions and policies, and escalate legal matters internally when appropriate.
  • Own and maintain the Global Site Contracts Library, including country-specific templates, guidance, and supporting materials.
  • Lead contract-template development, validation, maintenance, translation coordination, version control, and continuous improvement.
  • Deliver training and ongoing support on templates, contracting processes, governance, and escalation procedures.
  • Collaborate across functions to standardize contracting activities, improve operational excellence, maintain compliance, and evolve contracting tools.

Requirements

  • Master’s degree in law and at least 5 years of demonstrable experience as a qualified lawyer, preferably in a law firm or as an in-house legal counsel.
  • At least 5 years of relevant experience with a sponsor, clinical research organization, or pharmaceutical clients, preferably in clinical site contracting.
  • Strong negotiation and communication skills, including the ability to challenge stakeholders.
  • Ability to coordinate and collaborate across and within complex projects.
  • Excellent legal, financial, and/or technical writing skills.
  • Thorough understanding of the regulated clinical-trial environment and the drug-development process.
  • Knowledge of and ability to apply GCP/ICH and applicable regulatory guidelines.

Nice to have

  • Exposure to a pharmaceutical and/or CRO environment.

Culture & Benefits

  • Full-time employment.
  • Work within a global clinical research and healthcare intelligence organization.
  • Collaboration across site contracting, project management, operations, and legal stakeholders.

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