Opportunity for B. Pharma/ M. Pharma as a Safety Writer II at Thermo Fisher Scientific (WFH Position) – Apply Now

Thermo Fisher Scientific is expanding its team and currently hiring B. Pharma and M. Pharma graduates for the role of Safety Writer II. This exciting opportunity allows you to work from the comfort of your home while contributing to a global leader in scientific research and healthcare. Join Thermo Fisher Scientific and help shape the future of safety writing in a dynamic and innovative environment. Explore this rewarding career path and be part of a company that values your expertise and dedication. Apply today for the Work From Home Safety Writer II position at Thermo Fisher Scientific!

Job Description

You should have significant scientific or medical writing experience, thrive in project teams and be focused on delivering exemplary levels of customer service. Capable of concise and clear written and verbal communication you will be able to understand, interpret, analyze and present complex data and have a high attention to detail. As you may be working on multiple reports at the same time, you should have strong organizational skills, including the ability to prioritize work to ensure that strict timelines are adhered to. You must be comfortable with having direct interaction with clients, as you will be responsible for running meetings and managing review and comment resolution stages of document preparation.

Summarized Purpose

Responsible for the planning, coordination and delivery of safety writing services for multiple clinical trial and/or marketed product projects. Performs day-to-day safety writing and related activities within a highly regulated pharmacovigilance environment, driven by strict timelines. Activities include but are not limited to delivery of safety writing deliverables ranging from low to medium complexity through achievement of the following tasks: project management, data review, authoring, and quality review. May also support authoring of higher complexity deliverables. Effectively collaborates with various parties, including but not limited to: PVG project team members, wider PPD/Evidera project team members, client contacts and third-party vendors.

Essential Functions

• Conducts data review, authoring, and quality review tasks on, and project manages a wide range of clinical trial and marketed product safety writing deliverables. These include low complexity (e.g. line listing reports; Periodic Adverse [Drug] Experience Reports (PA[D]ERs)) and moderate complexity (e.g. Development Safety Update Reports (DSURs), Periodic Safety Update Reports (PSURs)/Periodic Benefit Risk Evaluation Reports (PBRERs), development Risk Management Plans (dRMPs)) deliverables.
• May additionally support authoring of high complexity (Risk Management Plans (RMPs), marketing authorization dossier content, customized safety writing deliverables and regulatory authority assessment report responses) deliverables under supervision from more senior staff. Uses multiple company and client systems. Interacts with project team members and clients.
• Operates in a lead capacity, serving as the primary point of contact for assigned safety writing deliverables. Provides assistance in the development of program and departmental procedural documents. Mentors less experienced staff.
• Ensures that assigned safety writing and project management tasks are conducted in accordance with company policies and procedures, contractual agreements and applicable regulations.
• Reviews regulatory/pharmacovigilance publications and information sources to keep updated on current regulations, practices and procedures.
• Participates in departmental initiatives.
• Performs routine project implementation and coordination activities for assigned safety writing projects, including leading kick-off meetings, managing communications and data requests, participating in client meetings, audits and inspections, and reviewing metrics and budgets.

Knowledge & Skills

• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).
• Advanced knowledge of Microsoft Office package.
• Task based project management experience and experience with interacting directly with clients.
• Good understanding and knowledge of aggregate safety report writing guidelines, and clinical trial and post-marketing pharmacovigilance.
• Experience of authoring device aggregate safety reports or clinical evaluation reports is preferable, although not essential.
• Must have a minimum of two years’ experience in authoring two or more of the following report/document types for medicinal products:
  1. DSURs (Development Safety Update Reports)
  2. PBRERs / PSURs (Periodic Benefit Risk Evaluation Reports / Periodic Safety Update Reports)
  3. PA(D)ERs (Periodic Adverse [Drug] Experience Reports)
  4. RMPs (Risk Management Plans)

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