• 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.