- Providing expert-level clinical consultation and support to business partners.- Preparing protocols, informed consent forms, clinical study reports, manuscripts and any other related documents as assigned.- Leading/participating in medical and scientific forums (e.g. advisory boards, scientific discussions and medical conferences). - Contribute to development and implementation of medical writing processes, templates, and style guides.- Review all relevant documents and interacts with functional leader and project manager to develop a thorough understanding of project timelines. - Maintain familiarity with current industry practicesand regulatory requirements that affect medical writing.- Developing high-quality content including: slide kits, advisory boards' reports, speaker training materials, educational symposia, and summaries of key literature.- Completing all of the above in compliance with ICH/ FDA/EMEA or other appropriate regulatory guidelines, in addition to departmental and corporate or client SOPs and style guidelines. - Acting in the capacity of a project manager for medical writing projects.- Attending internal technical team and client team meeting

• Development of Clinical documents (including, but not limited to study protocols and clinical study reports).• Abstracts, posters, presentations for scientific meetings, and manuscripts for publication in scientific journals, and coordinates the processes involved in submitting such documents to scientific meetings and journals.• Contribute to the development and implementation of medical writingprocesses, templates, and style guides. Perform online literature searches, Identify relevant target journals for manuscript submission• Review all relevant documents and interacts with the functional leaders and project manager to develop a thorough understanding of project timelines. • Maintain familiarity with current industry practices and regulatory requirements that affect medical writing