Senior Medical Writer

Veristat; Manila; Hybrid; PHP 1,200,000 - 1,800,000; Full time

Job summary

Veristat seeks a Senior Medical Writer with a safety focus for hybrid work in Manila. The role leads smaller projects, interfaces with clients, and supports larger engagements within a delivery team. A strong regulatory background is required, with experience in DSURs/PSURs/PBRERs/RMPs/PADERs and related reports.

You will edit and assemble complex documents, coordinate with biostatistics and medical affairs, and ensure compliance with applicable guidelines while meeting tight deadlines.

Qualifications

• Bachelor’s degree or higher in a scientific discipline with regulatory writing experience.
• 5+ years of regulatory writing experience with aggregate safety reports (DSURs, PSURs, PBRERs, RMPs, PADERs, ACOs).
• Knowledge of regulatory authority guidelines and health authority submission standards.

Responsibilities

• Lead on smaller projects and support larger engagements within delivery teams.
• Interface directly with clients and manage project timelines and expectations.
• Ensure quality and compliance of aggregate safety reports.
• Collaborate with cross-functional teams to gather data and develop summaries.

Skills

MS Word proficiency

Editing reports

Table creation & figure insertion

Regulatory writing

Collaboration across teams

Time management

Data synthesis & summary

Education

Bachelor’s degree in a scientific discipline

Job description

## Senior Medical WriterApply: Hybrid: Manila: Full time: Posted 4 Days Ago: R-202608864**Job Description:****Position Specific Overview** The Senior Medical Writer - Safety Focus is a major contributor to document authorship for a variety of aggregate safety reports within the safety service line. The Medical Writer - Safety Focus will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team. * 105+ approved therapies for marketing applications prepared by Veristat* 480+ oncology projects in the past 5 years* 350+ rare disease projects delivered in the past 5 years* Flexible, inclusive culture — 70% remote workforce, 66% women-led teams* Learn more about our core values here! **Education, Experience, Training, and Knowledge** * Bachelor’s degree or higher, in a scientific discipline strongly preferred* 5+ years of regulatory writing experience with aggregate safety report writing including: Development safety update reports (DSURs); Periodic safety update reports (PSURs); Periodic benefit-risk evaluations reports (PBRERs); Risk management plans (RMPs); Periodic adverse drug experience reports (PADERs); Addenda to clinical overviews (ACOs); Safety topic reviews* Understand regulatory authority guidelines and requirements to be able to lead an internal project team and anticipate the effects that writing practice conventions can have on the final product when seeking health authority approval/acceptance\\* Experience in the development of aggregate safety reports **Skills & Abilities:** * Proficiency with Microsoft Word skills (editing tools, creating, and modifying tables, and inserting figures) and document management techniques* Strong understanding of the document creation process and of the drug development lifecycle* Ability to work in a collaborative environment, be tolerant of differences in culture and beliefs, easily build relationships with others, openly share information, and willingly contribute toward accomplishment of team goals* Be action- and detail-oriented, always seeking new development opportunities to build knowledge and skills* Show flexibility to meet project needs as required by deadlines and to meet corporate goals and objectives* Remain knowledgeable of changes in the industry and adapt best practices* Demonstrate solid time management and other organizational skills* Ability to synthesize data across multiple data sources and documents to create summary reports* Ability to use logical arguments to persuade others when presenting ideas and suggestions but also respond positively to opposing views voiced by others* Develop professional relationships with clients to further the business relationship and maintain current industry knowledge* Ability to identify and institutionalize work practices that are most effective to ensure consistency in performance *Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.*