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PAREXEL International Corporation Job Title
Principal Consultant - Regulatory Affairs Generalist

Company
PAREXEL International Corporation

Job Description
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Parexel.com
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Principal Consultant - Regulatory Affairs Generalist
United States of America - Remote - Northeast
Date posted
08/06/2022
Job ID
82166BR
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Overview
Success Profile
Rewards
Responsibilities
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As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter – and keeping them there –your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small.
In return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. Plus, as member of Parexel Consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. Join our team, and you will design solutions for the complexities of an ever-changing global marketplace.
Full Time
Travel: Yes
Glassdoor Reviews and Company Rating
Success Profile
Check out the top traits we're looking for and see if you have the right mix.
Detail-Oriented
Proactive
Problem-Solver
Results-Driven
Organized
Multi-Tasker
"When submitting major market applications, it’s key to ensure that the technical integrity of all data meets regulated requirement standards. Parexel makes this possible with a diverse team of seasoned professionals who care about getting important medicines to patients. This is Regulatory Operations at its best."
Chris – Associate Director, Regulatory & Access
"In this role, I have had the unique opportunity to work with regulatory experts who are not only some of the most distinguished in their field, but are also some of the most compassionate people I know. I’ve been able to grow so much professionally by standing on the shoulders of giants!"
Riley – Regulatory Affairs Consultant
Rewards
Global Impact
We are one truly global team working together to propel each client´s journey ahead faster.
Balance
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
Collaboration
Work with industry leaders and subject matter experts.
Freedom
The ability to innovate, ask “what if” and try new solutions without fear of failure.
Variety
Opportunities to work on multiple accounts – never boring!
Management
Strong management with depth of experience working for global health authorities.
Responsibilities
Parexel’s Regulatory Consulting Services (RCS)
team is comprised of smart, passionate, and dedicated experts who are driven by the extremely important work they do to assist our clients in delivering new and innovative medical treatments for patients.  This talented team is growing, and we are seeking a Principal Regulatory Affairs Generalist.  If you are self-directed with excellent communication and influencing skills, and thrive in a fast-paced, dynamic environment where you will continue to learn and have a direct impact through your work, we would love to connect!
A Principal Regulatory Affairs Generalist will be a talented, seasoned, and motivated regulatory affairs leader with prior experience creating and executing global regulatory strategies aimed at the most efficient regulatory pathway for medical therapies.  You will have solid knowledge of US FDA regulatory requirements and procedures and have substantial experience in preparing and/or managing major regulatory submissions to FDA. You will also have strong knowledge of and demonstrated experience in FDA’s Pediatric Programs, Orphan Drug, and expedited development programs. As a Principal Regulatory Affairs Generalist, you will work with clients and internal cross-functional project teams in planning product development strategies and leading global regulatory submissions within the Clients’ portfolios. You will be well versed in regulatory requirements and will share your knowledge and regulatory advice with clients on key aspects of drug development.
As a Principal Regulatory Affairs Generalist, you will:
Liaise with clinical, nonclinical, CMC, and Client’s team members to develop and execute regulatory strategies aligned with Client’s business objectives. Provide guidance, direction, and leadership on those strategies to development teams and executive management
Lead teams in producing complex, global regulatory submissions to include review and approval of regulatory documents in support of filings including INDs, briefing materials for Health Authority (HA) meetings, pediatric plans, orphan drug applications, NDAs/BLAs, etc.
Lead teams to plan for critical HA meetings (e.g., Pre-IND, EOP2, pre-NDA/BLA); prepare for HA meetings including determining meeting objectives, key messages, and represent Clients with HAs including negotiations on complex issues related to early development
Manage complex projects from inception to completion to include providing regulatory guidance to help establish team goals, determining objectives, anticipating needs, initiating complex work, and leading others to drive complex, critical regulatory submissions to completion which align with Clients’ goals
Analyze and communicate current regulatory guidance and regulations, as well as industry and regulatory agency best practices and trends
Demonstrate excellent communication skills to present complex regulatory information
Ensure Clients are informed of any relevant changes in the regulatory landscape and Client’s regulatory strategies and product development activities are optimized. When necessary, draw upon your therapeutic and/or product expertise to propose effective and practical solutions
Thought Leadership
Delivers presentations at seminars and industry group meetings Authors articles for publication in industry magazines, newsletters, book chapters and other forums
May serve as a member of industry association boards, task forces and committees and/ or as chairperson or officer of one or more professional associations. Contributes expertise to professional societies, academic or other similar groups influential in his/ her area of expertise
Drives knowledge-centered activities within Parexel Consulting as well as contributes to Parexel business process improvements
Contribute to new RCS service and consulting model development
Business Development
Actively prospects and leverages new business opportunities with client and industry contacts in collaboration with Account Management
Presents information about Parexel Consulting service offerings reflecting the organization’s capability to support client needs
Generates new or repeat business due to personal name recognition or history of client satisfaction and/or relationship
Leverages rainmaking skills resulting in new and repeat business for Parexel. Is responsible for constant monitoring of his/her “A” list, and is expected to have continued contact with both existing and future potential clients
Participates in project scoping calls and proposal preparation
Delivers sales presentations and participates in bid defense meetings when needed
Actively participates in account planning for key clients
Other Parexel responsibilities
Meets established metrics as specified in scorecard on an annual basis
Completes basic job-related responsibilities, including timesheets, expense reports, maintenance of CVs, project deliverable archiving, participation in internal initiatives/projects or as a mentor as requested by management
Defines self-development activities to keep current within the industry (i.e., maintain membership in a relevant industry and/or scientific/technical association)
Participates in thought leadership activities (i.e., present speeches or seminars to industry groups and/or author articles.)
Skills
•          High-level consulting skills
•          Critical thinking and problem-solving skills
•          Project leadership and management knowledge
•          Excellent interpersonal and intercultural communication skills, both written and verbal
•          Client-focused approach to work
•          Results orientation
•          Teamwork and collaboration skills
•          Proficiency in local language and extensive working knowledge of the English language
•          Account planning and support
•          Networking
•          Business acumen and analysis
•          Self-confidence and control
Knowledge and Experience
10-15 years of experience with expert level industry or regulatory knowledge; experience with a regulatory agency (such as FDA, MHRA) is a plus
Education
Minimum of a Bachelor’s Degree in a Scientific or Technical Discipline, PhD or other advanced degree preferred
The ability to travel up to 30% domestically and/or internationally may be required
Employment is contingent on disclosure of your COVID-19 vaccination status and, if relevant, proof of vaccination.
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.
Apply Now
FAQ: Hiring during COVID-19
Learn how we recruit the best minds in these unprecedented times.
Learn More
Meet Stephanie: Associate Director, Regulatory & Access
Stephanie shares her story about her development within Parexel and what it's like to work here.
Learn More
Our hiring process
Find out what to expect when applying to Parexel
Learn More
Flexible Work Arrangement
In-office, home-based or a mix? What’s your preference? We value the work-life balance of our employees, and as such Parexel is offering maximum flexibility to our employees wherever possible.
Learn More


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