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Medical Writer, Belgium - L

Employer
ClinChoice
Location
Belgium
Salary
Competitive
Start date
30 Apr 2021
Closing date
27 May 2021

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Discipline
Medical Communications, Medical Writing
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Description:
TalentSource Life Sciences is currently searching for a Medical Writer to join one of our partner companies, in Walloon Brabant. Our client develops, manufactures and supports innovative equipment and software solutions for diagnostic, cancer treatment, and industrial applications.

As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client counter-parts.

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 continuous support from your TalentSource Line Manager.

Scope of the role:

Within the clinical solution team your main responsibility is to communicate complex medical information (related to oncology and proton therapy) in clear and compliant writing. The communication types can vary: clinical trial deliverables, clinical evaluation process deliverables or scientific reports.
Succeeding in this job is strongly communicating with meticulous attention to details and collaborating with the following departments: innovation & development, regulatory and clinical investigators.

Main Responsibilities:
  • Understanding the nature of the scientific work you will be covering
  • Writing, editing, and updating clinical development and evaluation related documents with the highest level of accuracy (clinical protocols, ….)
  • Developing a technical content that your audience or readers will understand
  • Providing critical analysis of the data you will gather


Education and Experience:
  • A master degree in scientific, medical or clinical discipline with at least 3 years of experience in medical writing
  • Experience in medical device environment is a plus
  • Experience with writing document compliant with ISO 14155 is a plus
  • Experience with MDR compliant clinical evaluation documentation like CER and CEP
  • A good knowledge of medical devices regulations concerning clinical investigations


Requirements and Skills:
  • Excellent written and verbal communication skills in English
  • Expert knowledge of the methods, techniques, and procedures of medical writing tasks
  • Proven track record in preparing clinical documents with minimum supervision
  • Familiarity with statistical and data output
  • Attention to details and the drive to get things done in an autonomous and proactive way
  • Good communication skills and team player
  • Ability to communicate scientific or medical information in a clear and concise manner
  • Proficiency in Word, Excel, PowerPoint, email, and the Internet


Our benefits when working in Belgium:
  • Competitive Salary
  • Group and hospitalisation insurance
  • Electronic meal vouchers
  • Internet reimbursement
  • Company Car with fuel card depending on the function
  • Dedicated Line Manager
  • Regular face-to-face or phone meetings with line manager
  • Full annual performance review process
  • Ad-hoc team events and end of year party
  • Career opportunities within both our CRO departments and our TalentSource Life Sciences Unit, locally and internationally
  • Employee satisfaction survey - your feedback is important for continuous improvement


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=HQ00002498

or please contact Vanessa.Verdickt@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.

Key words: Medical Writer
Skills: Medical Devices, Medical Writing, MS Office, statistical analysis 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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