
501 - 1000 employees
⥠Energy
đ€ Artificial Intelligence
Energy âą Artificial Intelligence âą Digital
TGS is a leading energy data and services company formed through the merger of PGS and TGS. It specializes in providing high-quality seismic and well data to clients across the energy value chain, enabling strategic partnerships and informed decision-making. TGS also offers carbon storage and monitoring solutions, wind and solar energy operations, and advanced imaging and digital services powered by analytics and AI. With decades of geoscience expertise, TGS is committed to innovation, sustainability, and supporting energy exploration and production worldwide.
đ„ 1 minute ago
Improve your chances of getting an interview by checking your resume score before you apply.

501 - 1000 employees
⥠Energy
đ€ Artificial Intelligence
Energy âą Artificial Intelligence âą Digital
TGS is a leading energy data and services company formed through the merger of PGS and TGS. It specializes in providing high-quality seismic and well data to clients across the energy value chain, enabling strategic partnerships and informed decision-making. TGS also offers carbon storage and monitoring solutions, wind and solar energy operations, and advanced imaging and digital services powered by analytics and AI. With decades of geoscience expertise, TGS is committed to innovation, sustainability, and supporting energy exploration and production worldwide.
âą Lead planning and preparation of high-quality clinical regulatory documents âą Produce protocols, publications, study reports, investigator brochures, narratives, and module documents according to client and agency guidelines âą Lead document execution, including creating, maintaining, and communicating timelines âą Coordinate cross-functional client contributors, stakeholders, and internal resources such as quality control and publishing âą Ensure document development follows client processes, templates, and instructional documents âą Serve as an expert on the client document management system, tools, templates, and procedures âą Lead document message development with clients âą Interpret data and create shell documents to support authoring âą Plan and lead kickoff meetings âą Facilitate review-feedback resolution and lead comment resolution meetings âą Follow up with team members to resolve outstanding review feedback âą Ensure consistency across client programs in messaging, formatting, and document presentation âą Conduct literature searches as needed âą Perform peer quality-control review as needed âą Contribute to medical writing operational initiatives such as templates, style guides, and reference management
âą 5+ years of experience as a medical writer in the CRO/biotech/pharmaceutical field âą Bachelorâs degree or higher in a relevant field âą Oncology, Infectious Disease, or Vaccine experience desired âą Experience writing clinical study reports, protocols, protocol amendments, investigator brochures, module 2, and module 5 documents desired âą Flexibility to work across multiple therapeutic areas, if needed âą Experience writing documents according to established processes and document templates âą Familiarity with lean authoring approaches and structured content management âą Familiarity with ICH and US regulatory requirements; working knowledge of ex-US regulatory requirements desired âą Expertise with Microsoft Word and other Microsoft applications âą Experience developing documents using document management systems, collaborative authoring tools, and review tools âą Comfortable adapting to new tools and technologies, if needed âą Ability to work independently and collaboratively amid competing priorities âą Service-oriented and proactive approach to project management âą Excellent conflict management and negotiation skills âą Comfortable providing suggestions based on previous experience âą Strong written and verbal communication skills in English âą Must be based in Poland and legally authorized to work there, as stated in the application questions
âą Equal employment opportunity regardless of race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law
Apply Nowđ 3 days ago
Principal Medical Writer creating complex clinical and regulatory documents for Syneos Health, a life sciences services organization. Advising sponsors, leading reviews, and mentoring medical writers.