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4 дня назад

Proposals Development Associate II (Late Phase/RWE)

Формат работы
remote (только USA)/onsite
Тип работы
fulltime
Грейд
middle
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
Proposals Development Associate II (Late Phase/RWE): Developing and coordinating proposals, budgets, and RFP responses for Phase IV, observational, registry, post-marketing, and real-world evidence research programs with an accent on clinical research methodologies, cross-functional collaboration, and client-focused deliverables. Focus on evaluating study and bid requirements, coordinating scientific and operational inputs, and ensuring accurate, compliant submissions under competing deadlines.

Location: Blue Bell, United States; remote or office-based work. Approximately 5% travel required.

Company

hirify.global is a global healthcare intelligence and clinical research organisation focused on bringing new medicines and treatments to patients faster.

What you will do

  • Collaborate with cross-functional teams to gather and analyze information for Phase IV, observational, real-world, registry, and evidence-generation studies.
  • Prepare, develop, format, and review proposals, budgets, and supporting documentation against client requirements and operational capabilities.
  • Support RFP evaluation and bid strategy by identifying study design, operational, and commercial considerations.
  • Coordinate input from clinical operations, biostatistics, data management, epidemiology, patient-centered outcomes, and HEOR subject matter experts.
  • Review proposal documents for accuracy, consistency, compliance, and alignment with client objectives.
  • Support proposal managers with timelines, milestone tracking, stakeholder coordination, and timely submission of deliverables.

Requirements

  • Bachelor’s degree in business, life sciences, public health, communications, or a related discipline.
  • Previous experience in proposal development, business development support, project coordination, or a related function within the pharmaceutical, healthcare, CRO, or clinical research industry.
  • Experience developing proposals and responding to RFPs for Late Phase, Real World Evidence, observational, registry, post-marketing, or non-interventional studies is strongly preferred.
  • Understanding of clinical research methodologies, including Phase IV studies, prospective and retrospective observational research, patient registries, and real-world data collection approaches.
  • Experience collaborating with cross-functional teams to develop client-focused proposals, budgets, and supporting documentation.
  • Strong attention to detail and organizational skills, with the ability to manage multiple proposal opportunities simultaneously under competing deadlines.
  • Excellent written and verbal communication skills, including the ability to convey complex scientific and operational information effectively.
  • Proficiency in Microsoft Office, particularly Word, Excel, and PowerPoint.
  • Willingness to travel as required, approximately 5%.

Culture & Benefits

  • Inclusive culture focused on integrity, collaboration, agility, belonging, and high performance.
  • Competitive salary and country-specific benefits.
  • Various annual leave entitlements, health insurance options, retirement planning, and life assurance.
  • Global Employee Assistance Programme with 24-hour access to a network of independent wellbeing professionals.
  • Optional benefits may include childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, and health assessments.

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