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Employer Sponsored Job (Free to apply to)
PAREXEL International Corporation Job Title
FSP Regulatory Affairs Consultant - CTR (flexible location UK/EU)

Company
PAREXEL International Corporation

Job Description
Parexel.com
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FSP Regulatory Affairs Consultant - CTR (flexible location UK/EU)
United Kingdom, Remote
Date posted
09/06/2022
Job ID
R0000002514
Apply Now
Overview
Success Profile
Rewards
Responsibilities
Map
Recent Jobs
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
We are currently looking for a Regulatory Affairs Professionals to join one of our clients and act as
 a (Senior)
Regul
atory Affairs Consultant CTR
This role can be based in either UK or UE (home/office based) and we have flexibility on levels.
In this role you will work closely with other departments to design, implement applications & systems to support regulatory business processes. You will work with key stakeholders to map current processes and organize task forces to define and implement process improvements. You will support the organization by analyzing (as business analyst) and managing and/or coordinating EU CTR process changes and organizational changes.
Role responsibilities:
Draw models for the business processes (process flows)
Moderate workshops with business experts
Ensure good communication with stakeholders in the project (verbally and written)
Draft new procedures based on new business processes & user requirements
Create training material and reference guides
Evaluate new system packages for
implementation
Write & run user test cases
Provide support to end-users
Design and generate reports for stakeholders
Liaise with other operational teams for system inter-operability
Work with external partners and authorities for data update and data exchange with authorities (e.g. EMA for XEVMPD, IDMP)
Ideal candidate will possess:
• University degree in a science discipline
A background in clinical trial management with a specific focus on EU CTR
• G
ood level of knowledge of the CTA business in addition, an expertise/skill in cross-functional project management and planning, process optimization
, and training.
• Project Management experience
• IT knowledge (Veeva Regulatory and Clinical Vaults - excel – VBA – powerBI…)
• Solid analysis and synthesis capability; Solution-oriented and problem-solving skills.
• Customer-oriented and autonomous
• Fluency in English is a must along with the local language.
#LI-REMOTE
Apply Now
FAQ: Hiring during COVID-19
Learn how we recruit the best minds in these unprecedented times.
Learn More
Our hiring process
Find out what to expect when applying to Parexel
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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
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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