<ul><li><span style="background-color:rgb(255,255,255);color:rgba(0,0,0,0.9);">Help in preparation of clinical trial related documents like synopsis, protocol, Risk Evaluation and Mitigation Strategies (REMS), Informed Consent Document (ICD).</span></li><li><span style="background-color:rgb(255,255,255);color:rgba(0,0,0,0.9);">Clinical Study Report (CSR), Common Technical Document (CTD), electronic CTD (eCTD) modules and any other document as needed for regulatory submission/requested by sponsor.</span></li></ul>

Junior Manager - Medical Writer