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パレクセルは、臨床開発の上流から下流までのそれぞれの専門領域で、国内外の多くのお客様に高度なソリューションを提供するプロフェッショナル集団です。 パレクセルは、新しい薬や治療法を、それらを必要としている人々にいち早く届けることを目指し、日々の業務に取り組んでいます。

Regulatory Affairs, Solutions Consultant/Solutions Strategist

求人ID 64234BR ロケーション アメリカ合衆国 仕事内容
Join Parexel's best-in-class Regulatory Consulting Team!

Are you a business savvy regulatory professional who is looking for an opportunity to use your technical expertise and tailor regulatory solutions to help clients overcome the demands of today's challenging regulatory landscape?

Are you looking for an opportunity to work in a truly global organization which offers full service solutions to clients?

Is the ability work alongside a highly recognized team of industry experts with exceptional technical knowledge and the ability to deliver operationally appealing?

If so, our Parexel Consulting team is growing! We currently have an amazing opportunity for a Regulatory Affairs, Solutions Consultant/Solutions Strategist/Architect, to join Parexel's Regulatory Consulting Team!

We are currently seeking an experienced regulatory professional or regulatory affairs proposal manager who will utilize principles and standards to drive and develop Parexel regulatory solutions to support life sciences clients. This individual will lead core services pursuit teams by leveraging best practices, appropriate SMEs and industry needs assessments; develop the market for Parexel in designated region/client grouping in line with business plan through developing senior client relationships; will achieve new business targets and oversee awarded projects to ensure client satisfaction and repeat business; and be responsible for project P&L roll-up for designated regional/client grouping, ensuring appropriate contribution to margin, and high quality deliverables.



Minimum Bachelor’s degree or equivalent in life sciences or technology-related discipline

Knowledge and Experience:

4+ years’ experience in a life sciences, pharmaceutical, industry-related consulting environment with an emphasis on Regulatory Affairs proposal development, past experience leading CTA applications, or experience with other clinical trial regulatory solutions.

• Significant pharmaceutical industry experience

• Regulatory, clinical research and/or product marketing

• Business development/consultancy

• Budget management

• A solutions focused/problem solving mindset

• Excellent written and oral communication skills

• A commitment to quality

Ability to travel 25-30%

EEO Disclaimer

Parexel is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.









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