Key Facts

Remote From:

Freelance

Senior (5-10 years)

Japanese, English

Hard Skills

Regulatory Compliance Regulatory Compliance Regulatory Compliance Vulnerability Scanning Veeva ISpring Suite Adobe Creative Cloud Documentum Diagramming Software Task Management

Other Skills

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Microsoft Excel
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Microsoft PowerPoint
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Microsoft Word
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Teamwork
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Adaptability
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Problem Solving

Roles & Responsibilities

At least 5 years in pharmaceutical industry (Sr. Associate), 8-10 years (Consultant)
Experience in eCTD publishing and document management
At least 3-5 years in global regulatory information management (Sr. Associate: 3 years, Consultant: 5 years)
Experience with regulatory technology (Documentum, Veeva Vault, etc.)
Proficiency in Microsoft and Adobe tools
Fluent in Japanese and English

Red Nucleus

Pharmaceuticals

About Red Nucleus

We are a global strategic partner with decades of experience across the entire life sciences product lifecycle. We excel in providing our clients with unique insights and efficiencies to support them in their journey to improve health outcomes and ultimately the quality of people’s lives. By connecting our full suite of products and services from scientific and advisory services, market access, medical communications and learning and development, we are the “red thread” to lead our life sciences clients through transformational change to accelerate customer success. Visit the new rednucleus.com to learn more.

Company type: SME

Industry: Pharmaceuticals

Founded: 2018

Company size: 501 - 1000

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Job description

COMPANY DESCRIPTION: Red Nucleus is the premier provider of strategic learning, performance, and process solutions exclusively for the life sciences industry. Our global solutions engage and inspire teams across the R&D, Medical Communications, and Commercial spaces and are designed to boost understanding, efficacy, and compliance. Squarely focused on the life sciences industry for more than 30 years, Red Nucleus takes pride in our long-term relationships with industry leaders, as well as our strategic partnerships with innovative startups. We are focused on developing thoughtful, high-quality solutions that are in accordance with each client's unique culture and process. Our clients trust us to build impactful, award-winning programs that deliver actionable insights and measurable results.

Our purpose at Red Nucleus is advancing knowledge to improve lives. We succeed by being the premier provider of strategic learning and development, scientific and strategic advisory services, and medical communications solutions for the life sciences industry. Our global team is composed of nearly 900 full-time employees whose commitment to creativity, quality, and on-time delivery is unrivaled in our space.

Job Title: Sr. Associate Consultant or Consultant

Key Skills/Phrases:

Regulatory Operations

At least 5 years (Sr. Associate), 8-10 years (Consultant) of experience in the pharmaceutical industry with a focus in Regulatory O
At least 5 years (Sr. Associate), 8-10 years (Consultant) of experience eCTD publishing, submitting and managing documents for major submissions including electronic study data.
At least 3 years (Sr. Associate), 5 years (Consultant) of experience with global regulatory information management and systems.
Experience assisting with the implementation of a regulatory technology such as, Documentum, Veeva Vault, Insight Manager, Insight Publisher, docuBridge, etc.
Proficient in Microsoft Excel, Word, PowerPoint, Visio and in Adobe Acrobat, Evermap or ISI Toolbox, and eCTD publishing tool.
Fluent in Japanese and English languages

Desired Attributes:

Ability to adapt to the flexibility and fast-paced environment of a global company
Capability to manage multiple tasks simultaneously
Ability to work collaboratively as part of a team to drive projects forward
Proactive approach to problem-solving

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