Consultant / Sr. Consultant - Scientific Writer

As a Consultant / Sr. Consultant - Scientific Writer, your role involves preparing literature reviews, abstracts, posters, slide sets, and manuscripts (complex) by working with various data sources such as clinical study reports and patient profiles. You are responsible for performing quality control (QC) checks and proofreading of the deliverables to ensure they meet customer expectations. It is essential for you to comply with and support the group's project management tools, standards, policies, and initiatives. Maintaining records for all assigned projects, including archiving, and ensuring audit, SOP, and training compliance are also key responsibilities. - Prepare literature reviews, abstracts, posters, slide sets, and manuscripts using data from clinical study reports and patient profiles - Perform quality control (QC) checks and proofread deliverables to meet customer expectations - Comply with project management tools, standards, policies, and initiatives - Maintain records for assigned projects, including archiving and ensuring audit, SOP, and training compliance Qualifications Required: - Expertise in literature review, abstracts, posters, slide sets, and manuscripts - Attention to detail and ability to meet customer expectations If you have a passion for scientific writing and possess the necessary skills in literature review, abstracts, posters, slide sets, and manuscripts, we encourage you to apply for this full-time, permanent position in the ITES/BPO/KPO industry under the functional area of Pharmaceuticals. The role falls under the outsourcing/Offshoring category.,