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Regulatory Affairs Expert, Brussels, Belgium - L

Employer
ClinChoice
Location
Belgium
Salary
Competitive
Start date
8 Sep 2020
Closing date
7 Oct 2020

View more

Discipline
Regulatory Affairs
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Description:
TalentSource Life Sciences, a division of CROMSOURCE, is currently seeking an enthusiastic Team Player, to join a Global, leading pharmaceutical company located in Brussels, Belgium.

The Regulatory Affairs Expert supports the Regulatory Lead in planning and executing the necessary regulatory activities to progress the Project portfolio with the ultimate aim of obtaining marketing authorisations globally.

Responsibilities
  • Contact person for assigned responsibilities on the product, in alignment with Regulatory Lead
  • Assume responsibilities for contact with 3rd party partners (mainly CROs), building strong relationships for assigned project(s), in line with the Regulatory Lead
  • Responsible for providing regulatory expertise and strategy, in alignment with the Projects
  • Support and deliver quality regulatory submissions in line with the applicable regulations, directives and guidelines, and in line with agreed strategies and timelines.
  • Ensure that all documents and information are adequately captured in a timely fashion in the applicable systems (document management, databases, etc).
  • Prepare and communicate regulatory strategic and operational plans for assigned projects
  • Maintain awareness of external regulatory environment, new guidelines and legislation


Requirements
  • Experience of EU regional regulatory procedures and legislation related to drug development and clinical trial applications. From 5 to 10 years of global experience preferred in this field.
  • Strategic and results focused - ability to overcome obstacles and achieve key outcomes
  • Strong Project planning and management skills, being able to perform risk assessments, anticipating problems and providing creative solutions.
  • Analytical - logically breaking situations or issues down into their essential elements: carrying out diagnosis and developing solutions
  • Integrity - overriding commitment to integrity and high standards in self and others
  • Flexibility and adaptability - Decides what to do based on the situation. Changes behavior or approach to fit the situation or the person. Works effectively in ambiguous situations.
  • Facilitates and coordinates teams and processes with appropriate use of interpersonal skills
  • Build effective partnerships - identifies opportunities and takes actions to build effective relationships within team and with other areas
  • Influencing skills - through well thought through rationale and effective communication skills, able to influence key decisions
  • Communication skills - knows when and how to communicate, using strong interpersonal skills and written communications when appropriate
  • Sensitivity to the diverse cultures comprising- the international and global environment


Our benefits when working in Belgium
  • Dedicated Line Manager
  • Monthly meetings with line manager
  • Employee satisfaction survey - your feedback is important for continuous improvement
  • Annual appraisals development planning
  • Yearly team event
  • New Year's diner
  • Group and hospitalisation insurance
  • Electronic meal vouchers
  • Internet reimbursement


Who will you be working for?

About CROMSOURCE

CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.

Our Company Ethos

Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values are evidenced by our below industry average turnover rates.

About TalentSource Life Sciences

TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having the continuous support from your Line Manager, who will work closely with you to mentor and support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role and work autonomously.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

If you would like to discuss the role before applying through the website @ https://www.talentsourcelifesciences.com/job-information/?job-id=HQ00002239

or please contact Rocio.EgeaMota@cromsource.com for more information.

CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Keywords: Regulatory Affairs Expert, EU regional regulatory procedures, Global Regulatory Affairs, Drug Development, Marketing Authorisation, Contract Research Organisation, CRO, BioPharma, Pharmaceuticals, Clinical trials
Skills: Regulatory Location: Belgium Share:

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Company

ClinChoice

ClinChoice is a recognized and highly respected mid-size, global, full-service contract research organization (CRO) specializing in clinical development, post-marketing, and functional service support. We provide comprehensive end-to-end solutions, taking products from early clinical development to post-approval lifecycle management. We are committed to fostering innovation in the pharmaceutical, biotechnology, medical device & diagnostics, consumer health, cosmetics, and nutraceuticals industries. Since our establishment in 1995, we have consistently delivered high-quality services and solutions throughout the entire development lifecycle of our clients’ products. We serve a wide-ranging clientele that encompasses six of the top ten pharmaceutical companies, leading medical device companies, preeminent biotechnology companies, the largest consumer health and cosmetics companies, and numerous small-to-mid-sized innovator companies. With over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific, we are positioned to fulfil our clients’ needs locally and globally.

 

We’re on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

 

Company info
Website
Telephone
+44 1628 566121
Location
Suite G48
268 Bath Road
Slough
Berkshire
SL1 4DX
United Kingdom

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