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Safety Writer II

EXTRA HOLIDAYS - EXTRA PARENTAL LEAVE
Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Bachelor's or higher scientific degree, Excellent written and verbal English skills, Advanced knowledge of Microsoft Office, Task-based project management experience, Minimum two years' experience in authoring safety reports.

Key responsabilities:

  • Understand, interpret, and analyze complex data
  • Write concise and clear reports and documents
  • Manage multiple reports simultaneously
  • Facilitate meetings and manage document preparation stages
  • Interact with clients and provide exceptional customer service
Thermo Fisher Scientific logo
Thermo Fisher Scientific Biotech: Biology + Technology Large https://www.thermofisher.com/
10001 Employees
HQ: Waltham
See more Thermo Fisher Scientific offers

Job description

Logo Jobgether

Your missions

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

About Thermo Fisher Scientific Inc.

Thermo Fisher Scientific Inc. is a global leader in the life science sector, providing world-class solutions to pharmaceutical companies, biotech companies, and Clinical Research Organizations (CROs). As the trusted partner of some of the most innovative big pharma and biotech companies, we offer exceptional opportunities for experienced Safety Writers to work on exciting projects across a wide range of therapeutic areas.

As a Safety Writer at Thermo Fisher Scientific, you will play a crucial role in ensuring the flawless delivery of scientific and medical writing services. You will thrive in project teams, delivering outstanding levels of customer service and collaborating with clients to successfully conduct projects. Your responsibilities will include:

  • Understanding, interpreting, analyzing, and presenting complex data
  • Writing concise and clear reports and documents
  • Managing multiple reports simultaneously and prioritizing work to meet strict timelines
  • Facilitating meetings and managing the review and comment resolution stages of document preparation
  • Interacting directly with clients and providing exceptional customer service

Job Requirements

To qualify for this position, you must possess the following qualifications:

  • Bachelor's or higher scientific degree
  • Excellent written and verbal English interpersonal skills
  • Advanced knowledge of Microsoft Office package
  • Task-based project management experience and experience with client interaction
  • Good understanding and knowledge of aggregate safety report writing guidelines, clinical trial, and post-marketing pharmacovigilance
  • Experience authoring device aggregate safety reports or clinical evaluation reports is preferable

In addition, you must have a minimum of two years' experience in authoring two or more of the following report/document types for medicinal products:

  • DSURs (Development Safety Update Reports)
  • PBRERs / PSURs (Periodic Benefit Risk Evaluation Reports / Periodic Safety Update Reports)
  • PA(D)ERs (Periodic Adverse [Drug] Experience Reports)
  • RMPs (Risk Management Plans)

Our Offer

At Thermo Fisher Scientific, we offer a positive and supportive working environment within one of the most engaged teams in the industry. We recognize our employees as the cornerstone of our success and provide opportunities for personal and professional growth. In addition, we offer a driven remuneration package and corporate training.

To apply for this position, please submit your CV in English through our website.

Please note that only short-listed candidates will be contacted.

Thermo Fisher Scientific is an equal opportunities employer.

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Biotech: Biology + Technology
Spoken language(s):
Check out the description to know which languages are mandatory.

Hard Skills

Soft Skills

  • non-verbal-communication
  • microsoft-office
  • report-writing
  • Customer Service
  • Time Management

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