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Regulatory Affairs, Solutions Consultant/Solutions Strategist
応募 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%
応募あとで応募 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.
Qualifications
Education: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%