Назад
Company hidden
4 дня назад

Associate Director, Preclinical Sciences and Translational Safety (PSTS) Integration & Transition Management (MedTech)

137 000 - 235 750$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US/Belgium
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/
TL;DR
Associate Director, Preclinical Sciences and Translational Safety (PSTS) Integration & Transition Management (MedTech): Leading cross-functional integration and transition programs for acquisitions, licensing transactions, collaborations, investments, and divestitures across preclinical and translational safety operations with an accent on diligence handoffs, data and records migration, compliance, facilities, CROs, and financial planning. Focus on coordinating Day 1 and long-term integration readiness, managing risks and dependencies, and translating complex scientific, operational, and regulatory requirements into executable plans.

Location: Hybrid role based in Spring House, Pennsylvania, or La Jolla, California, United States; an equivalent posting is available in Beerse, Belgium.

Salary: $137,000–$235,750 annual base pay.

Company

Johnson & Johnson MedTech develops healthcare solutions and innovative medicines focused on preventing, treating, and curing complex diseases.

What you will do

  • Lead PSTS integration planning and execution for acquisitions, licensing transactions, collaborations, strategic investments, options, and divestitures.
  • Translate diligence findings and transaction commitments into workstreams with owners, timelines, dependencies, decision points, and deliverables.
  • Coordinate Day 1, Day 100, transition, and long-term integration readiness across scientific operations, quality, safety, data, facilities, vivaria, CROs, budgets, and resources.
  • Coordinate the transfer and governance of preclinical records, electronic data, SEND packages, samples, materials, archives, systems, and study inventories.
  • Manage assessments involving GLP and non-GLP studies, regulatory requirements, animal welfare, AAALAC accreditation, NHP work, facilities, CROs, vendors, and business continuity.
  • Develop executive dashboards, monitor milestones, risks, issues, budgets, and dependencies, and present recommendations to senior leadership.

Requirements

  • Minimum bachelor’s degree in a scientific, technical, operational, business, or related discipline.
  • Minimum 8 years of relevant experience in pharmaceutical, biotechnology, CRO, research, or life sciences environments.
  • Experience leading complex cross-functional programs, integration workstreams, strategic initiatives, or large-scale transitions in a matrixed organization.
  • Working knowledge of preclinical research operations, quality and compliance, regulatory documentation, CRO/vendor oversight, and data or records transfer.
  • Strong capabilities in program management, governance, risk identification, issue resolution, executive communication, financial planning, and decision facilitation.
  • Ability to influence without direct authority and operate effectively amid ambiguity, changing priorities, compressed timelines, and incomplete information.

Nice to have

  • Advanced degree such as an MS, PhD, DVM, PharmD, MBA, or equivalent.
  • Experience supporting mergers and acquisitions, licensing, collaborations, business development transactions, or organizational transformation.

Culture & Benefits

  • Inclusive work environment guided by the company’s Credo and focused on patient impact.
  • Eligibility for pension, 401(k), savings, and long-term incentive programs.
  • Paid vacation, sick time, holidays, personal and family time, parental leave, bereavement leave, caregiver leave, volunteer leave, and military spouse time off.
  • Accommodation support is available during the interview process for applicants with disabilities.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →