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4 дня назад

Therapeutic Strategy Lead (IMM)

Формат работы
remote (только Europe)
Тип работы
fulltime
Грейд
lead/director
Английский
b2
Страна
UK/Serbia/Spain +7 еще
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
Therapeutic Strategy Lead (IMM) (Clinical Research): Developing and implementing therapeutic delivery strategies for customer proposals and clinical research programs with an accent on clinical operations, regulatory requirements, commercial strategy, and biopharma expertise. Focus on leading bid defense activities, guiding project teams, balancing internal and external data, and ensuring feasible strategies, quality, and financial performance.

Location: Home-based in Reading, Berkshire, United Kingdom, with additional locations in Belgrade, Serbia; Lisbon, Portugal; Budapest, Hungary; Athens, Greece; Barcelona, Spain; Prague, Czech Republic; Sofia, Bulgaria; Copenhagen, Denmark; Madrid, Spain; and Bucharest, Romania.

Company

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

What you will do

  • Develop and implement delivery strategies tailored to customer needs during RFP and bid defense cycles.
  • Collaborate with Sales, Medical, Operations, and other functions to create feasible, differentiated proposals.
  • Analyze therapeutic, operational, market, and competitive data to build long-term project strategies.
  • Enable project delivery teams to understand and implement sold project strategies.
  • Mentor Project Leaders and support customer, sales, and bid defense meetings.
  • Identify quality issues, coach corrective and preventive actions, and ensure project budgets support company goals.

Requirements

  • Bachelor's degree in life sciences and relevant global clinical research experience at director level.
  • Hands-on experience in operational delivery and/or drug development within the applicable IMM therapeutic area.
  • Deep knowledge of clinical operations, real-world research, regulatory requirements, commercial strategy, and the biopharma industry.
  • Knowledge of Good Clinical Practice and International Conference on Harmonization guidelines.
  • Strong business acumen, negotiation, influencing, customer management, presentation, and leadership skills.
  • Good command of written and spoken English is required. Prior experience in the Clinical Research Organization industry is required.

Nice to have

  • Proficiency in Mandarin.
  • Strong experience leading virtual teams in matrix organizations.
  • Strong software and Microsoft Office skills.

Culture & Benefits

  • Home-based work arrangement.
  • Inclusive culture focused on diversity, belonging, and collaboration.
  • Opportunity to support the development and commercialization of innovative medical treatments.

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