Match score not available

Safety Writer II

Remote:

Full Remote

Contract:

Full time

Experience:

Mid-level (2-5 years)

Work from:

India

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 in relevant report types.

Key responsabilities:

Analyze and present complex data
Write concise reports and documents
Manage multiple reports and prioritize work
Facilitate meetings and manage document reviews
Interact with clients and provide exceptional service

Lifelancer Information Technology & Services Startup https://lifelancer.com/

11 - 50 Employees

See more Lifelancer offers

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

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 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.

Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

https://lifelancer.com/jobs/view/1a3f221d1a8eebd5049e13e6b52d040e