Consultant / Sr.Consultant - Scientific Writer

Role Overview: As a Consultant / Sr. Consultant - Scientific Writer, your main responsibility will be to prepare literature reviews, abstracts, posters, slide sets, and manuscripts (complex) by collaborating with various data sources like clinical study reports and patient profiles. You will need to ensure the quality of the deliverables through performing QC checks and proofreading to meet customer expectations. Additionally, you are expected to adhere to the group's project management tools, standards, policies, and initiatives. Keeping records for all projects, including archiving, and ensuring compliance with audits, SOPs, and training are also part of your key duties. Key Responsibilities: - Prepare literature reviews, abstracts, posters, slide sets, and manuscripts - Collaborate with clinical study reports and patient profiles for data sources - Perform quality control (QC) checks and proofreading of deliverables - Adhere to project management tools, standards, policies, and initiatives - Maintain records for all projects, including archiving - Ensure compliance with audits, SOPs, and training Qualifications Required: - Expertise in literature review, abstracts, posters, slide sets, and manuscripts - Attention to detail and ability to meet customer expectations Company Details: The role is a full-time, permanent position in the ITES/BPO/KPO industry within the functional area of Pharmaceuticals. It falls under the outsourcing/Offshoring category. 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 position. *Job Code: GO/JC/21340/2025 *Recruiter Name: Mithra D,