Safety Writer III
at Thermo Fisher Scientific
zdalnie, województwo śląskie, Poland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 29 Jan, 2025 | Not Specified | 30 Oct, 2024 | 2 year(s) or above | Good communication skills | No | No |
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Description:
JOB DESCRIPTION
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.
Job Description
As a Safety Writer III 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 RMP and aggregate safety report writing guidelines, clinical trial, and post-marketing pharmacovigilance
In addition, you must have a minimum of two years’ experience in authoring the following report/document types for medicinal products:
EU RMPs and Core RMPs for innovative medicinal products (experience in authoring the full document is a requirement).
DSURs (Development Safety Update Reports)
PBRERs / PSURs (Periodic Benefit Risk Evaluation Reports / Periodic Safety Update Reports)
PA(D)ERs (Periodic Adverse [Drug] Experience Reports)
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
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Content, Journalism, Clinical Pharmacy
Graduate
Proficient
1
zdalnie, Poland