Anusha Mohan

Anusha Mohan

Project Management Analyst (CDM, Project Management Operations) - Pharma Domain

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location of Anusha MohanBengaluru, Karnataka, India

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  • Timeline

  • About me

    Senior Clinical Data Coordinator - Clinical Research & Trials

  • Education

    • St Joseph Post Graduate and Research Center(Autonomous), Bangalore

      2012 - 2015
      Master of Science - MS Microbiology, General
    • Jyothi Nivas college, Hosur Rd, Bangalore-95(Autonomous)

      2009 - 2012
      Bachelor of Science - BS Chemistry, Botany, Zoology
  • Experience

    • Accenture Bangalore

      May 2017 - Mar 2019
      Project Management Analyst (CDM, Project Management Operations) - Pharma Domain

      Lead and provide expert technical leadership to highly visible, sensitive and multi-faceted innovation projectsProject Scoping –investigate and understand the initial objectives set. Challenge the frame, where necessary, to ensure the right balance of business value with a realistic project.Sets strategic direction of projects. Develop standard operating procedures and ensure stakeholders are informed.Develops project plans which identify key issues, problems, approaches, performance metrics and resources required.Responsible for both strategic and tactical management of assigned projects.Lead project teams and manage work plans for each phase of the project including time lines, risk management and resource allocation.Develop and maintain constructive and cooperative working relationships with all stakeholders.Motivates team members and facilitates meetings by bringing all cross functional teams to a simple platform.Produce technical documentation including work instructions where applicable.Conduct field surveys to evaluate operations and recommend changes.Ability to conduct root cause analysis, employ techniques to identify and control sources of variation inherent in a process and derive solutions that are cost effective and meet service requirements.Use Microsoft Project Professional (MSP) tool to drive the projects by creating live networks.Develop training program for different levels of audiences for process improvements.Ensure best practice sharing and continuous improvement within the region. Analyzing data for highly confidential clinical trials. Analyze future and current end user requirements to improve clinical operations Design clinical and administrative reports. Support facilitating interdepartmental performance improvement activities. Proficient in defining and validating protocols for clinical studies and handling trial responsibility throughout the data-management life cycle. Show less

    • Accenture

      May 2017 - Mar 2018
      Project Manamgement Associate - CDM

      -Design clinical and administrative reports. -Proficient in defining and validating protocols for clinical studies and handling trial responsibility throughout the data-management lifecycle. -Ability to quickly master the industry best practices in clinical-study procedures and data management. -Excelled in managing high-priority projects and resolving data discrepancies, errors and omissions with thoroughness and precision. -Facilitated the rollout of new SOP that streamlined data entry and improved data-analysis functions. Contributed to design and development of new SOP compliance and validation components and reporting tools. -Ensures projects are conducted in compliance with operating procedures and good clinical practices. -Served as a primary trainer to peers on clinical studies. -Perform timely internal audits to maintain the integrity of clinical trials. Show less

    • Richmond Pharmacology - London

      May 2019 - Aug 2020
      Data Manager Associate

      The role involves -Supporting early phase of clinical study activity in the Data management team.-Uploading and Quality managing the delivery of data from specific ongoing clinical trials to the wider business. -A key role fundamental to the successful analysis and reporting of study data to the business and ultimately to the study sponsors and clients.-Assist with all data management activities including project set up ,creation of the Data handling protocol.-Designing of the case report form as per sponsor study requirement.-Assisting with quality control checks such as safety data preparation and performing data administration.-Data reconciliation and Medical coding using MedDRAof the AE’s during study lock. -Query analysis and management-Updating the trial master files and study documents ensuring they are complete and accurate-Extensive use of multiple EDC system as per sponsor requirement. Show less

    • IQVIA

      Oct 2020 - now
      • Senior clincal data coordinator

        Apr 2022 - now
      • Clinical Data Specialist

        Oct 2020 - now
  • Licenses & Certifications