8 часов назад
Sr Associate Project Manager - Remote (Biosimilars)
89 168 - 120 639$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Sr Associate Project Manager - Remote (Biosimilars) (project management, analytical similarity): Managing sample workflows and project coordination for biosimilar candidates progressing toward regulatory approval with an accent on inventory planning, laboratory database management, and data verification. Focus on coordinating cross-functional scientific teams, distributing samples for testing, organizing LIMS and ELN data, and ensuring regulatory document accuracy.
Location: United States - Remote
Salary: $89,168.40–$120,639.60 per year
Company
is a biotechnology company developing and manufacturing medicines for serious diseases across oncology, inflammation, general medicine, and rare disease.
What you will do
- Provide project management for technical teams developing biosimilar candidates through regulatory approval.
- Manage analytical similarity samples, inventory planning, sample distribution, and incoming project data.
- Coordinate with Similarity, Critical Reagents, Data Management, and scientific teams.
- Create electronic laboratory notebooks and manage sample submissions, work orders, and controlled document archives.
- Query LIMS, ELN, and other databases; organize and retrieve data for review and verification.
- Verify data in internal and regulatory documents and format materials according to internal standards.
Requirements
- Master’s degree, or a bachelor’s degree plus 2 years of project management experience.
- Alternatively, an associate’s degree plus 6 years of project management experience, or a high school diploma/GED plus 8 years of project management experience.
- Strong analytical, organizational, communication, Microsoft Word, and Microsoft Excel skills.
- Knowledge of good data practices, data verification, collaboration systems, and document management.
- Ability to manage multiple priorities and collaborate across scientific and regulatory functions.
Nice to have
- Experience supporting pharmaceutical research and development or nonclinical drug development programs.
- Experience with document management systems, collaboration platforms, project management tools, LIMS, or ELN software.
- Experience coordinating scientific or regulatory documents throughout their lifecycle.
- Bachelor’s or advanced degree in life sciences, regulatory affairs, business, or a related field.
Culture & Benefits
- Employee health, dental, vision, life, disability, and flexible spending benefits.
- Retirement and savings plan with company contributions.
- Discretionary annual bonus and stock-based long-term incentives.
- Paid time off and biannual company-wide shutdowns.
- Career development opportunities and flexible work models where available.
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 →
Похожие вакансии
3 дня назад
Assistant Project Manager
58 000 - 85 000$
3 дня назад
Clinical Supply Chain Project Leader (Biopharma)
105 000 - 151 666$
4 дня назад
Senior Project Manager
70 000 - 75 000$
10 часов назад
Associate Project Manager - Healthcare Advertising
53 500 - 66 900$
4 дня назад
Sr. Clinical Trial Manager, Therapeutics and Oncology
130 800 - 209 400$
4 дня назад