Назад
Company hidden
21 час назад

Scientific Director II, Oncology Early Development

182 000 - 346 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
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
Scientific Director II, Oncology Early Development (Clinical Development/Oncology): Leads the design, implementation, analysis, and reporting of clinical development programs and trials supporting oncology medicines with an accent on scientific strategy, regulatory compliance, and cross-functional collaboration. Focus on interpreting safety and efficacy data, developing protocols and regulatory submissions, overseeing study integrity and timelines, and guiding translational and clinical development activities.

Location: Florham Park, New Jersey, United States

Salary: $182,000–$346,000 per year

Company

Biopharmaceutical organization focused on discovering and delivering medicines and solutions for serious health issues, including oncology.

What you will do

  • Lead the design and implementation of multiple clinical development programs or one large, complex program.
  • Direct clinical study teams, monitor study integrity, and interpret and communicate accumulating safety and efficacy data.
  • Own the scientific content of protocols, Investigator Brochures, clinical study reports, regulatory submissions, and responses.
  • Develop cross-functional Clinical Development Plans and contribute to Integrated Evidence Strategy Teams and Asset Development Teams.
  • Coordinate scientific and medical activities for oncology molecules and diseases with internal stakeholders and external opinion leaders.
  • Support translational strategies, business development diligence, regulatory discussions, and adherence to Good Clinical Practices and pharmacovigilance standards.

Requirements

  • Bachelor's degree in a scientific discipline; an MS, PhD, or PharmD is preferred.
  • At least 5 years of clinical trial experience in the pharmaceutical industry, academia, or an equivalent setting.
  • Experience with clinical trial methodology, regulatory and compliance requirements, clinical strategy, and study protocol design.
  • Ability to oversee moderately complex clinical research programs with minimal supervision.
  • Ability to provide direction, collaborate across global cross-functional teams, and support scientific and business strategy.
  • Excellent written and spoken English communication skills are required.

Culture & Benefits

  • Paid vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) benefits for eligible employees.
  • Eligibility to participate in long-term incentive programs.
  • Equal opportunity employment and a workplace committed to integrity, innovation, and community service.

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 →