<ul><li>Prepare and review study related documents i.e. Protocol, ICD, CRF and related all other documents are part of regulatory submission.</li><li>Performing medical writing activities that support preparation of clinical study and regulatory documents required for drug development and registration activities.</li><li>Performing Project Coordination, Project Planning and its Execution and Management.</li><li>Familiarity with relevant software and technology used in clinical research, such as Electronic Data Capture (EDC) systems and statistical analysis software.</li><li>Commitment to staying informed about advancements in the field through continuous education and professional development.</li><li>Strong analytical and critical thinking skills to assess and interpret scientific literature and study results.</li><li>Commitment to ethical conduct in clinical research, including participant safety, informed consent, and data integrity.</li></ul>

Clinical Research Scientist