Mohamed Khamith Amirdeen

Experience

• 

  Cognizant

  Jan 2017 - May 2021

  Worked with global team as Lead programmer, managing study build and programming activities. • Manages trials as a Study Setup Trial Lead.• Communicates with client and data management team to understand the requirements and provide solutions.• Handles study related queries raised by client and the study team.• Manages the overall quality of deliverables and daily allocations of the team.• Analyze and resolved Post-Production issues.• Handle Post-production amendments.• Involved in process Improvement calls and provide suggestions.• Responsible for creating custom SAE reports based on client requirement using Crystal Reports and SQL.• Mentored any new joiners on the project/application process and the study setup activity. Show less • Managed trials as a Study Setup Trial Lead.• Communicated with client and data management team to understand the requirements.• Managed the overall quality of deliverables and daily allocations of the team.• Completed Daily programming tasks assigned and assisted fellow team members when required.• Analyzed and resolved Post-Production issues.• Handle Post-production amendments.• Attended meetings as required and ensured activities were completed on time. Show less

  • Associate

    Oct 2020 - May 2021

  • Programming Analyst

    Nov 2017 - Oct 2020

  • Programmer Analyst Trainee

    Jan 2017 - Nov 2017
• 

  PPD

  May 2021 - Apr 2023

  CDM Programmer II

  Worked with clinical data management systems and programming tools to provide advanced programming support in data management activities and deliverables including, but not limited to, database development and data validations, and assisted with defining tools and techniques for improving process efficiencies. Worked within a multi-disciplinary project team to complete assigned tasks on time and within budget. • Performed tasks following within the timelines established by the team, in accordance with the process outlined in the departmental procedures and indicated by the project contract.• Designed, built, and tested project databases, edit checks & custom functions.• Performed programming activities in line with project requirements.• Acted as the lead on studies. Researched and leveraged resources to resolve issues and manage complex tasks through the development and application of new knowledge and/or professional skills in areas including programming and technology.• Participated in process improvement initiatives to increase efficiencies.• Ensured adherence to departmental working practice documents and SOPs and contributed to the development of training materials. Show less

• 

  Thermo Fisher Scientific

  Apr 2023 - now

  Sr. CDM Programmer I

  Worked with clinical data management systems and programming tools to provide advanced programming support in data management activities and deliverables including, but not limited to, database development and data validations, and assisted with defining tools and techniques for improving process efficiencies. Worked within a multi-disciplinary project team to complete assigned tasks on time and within budget. • Act as the study lead, work directly with project team leaders and sponsors to conduct team meetings, develop, and maintain project timelines, assess, and forecast resources and monitor study budgets.• Lead requirement gathering sessions with sponsors to map the requirements, troubleshoot and provide custom solutions as per the requirement.• In-depth knowledge in designing CRF’s, and testing project databases, edit checks & custom functions, Post Go-Live changes implementation, Migrations and Quick publish, Site & User Admin and Lab admin module.• Sound knowledge in TSDV Configuration and related reports.• Part of the Rave Safety Gateway SME global team which make improvements in RSG process and standards practices followed during RSG programming.• Serve as SME in Custom Function Programming and Lab admin module across global team.• Part of the Global Library team, responsible for creating and maintaining global library templates for studies of various therapeutic areas.• Conduct training and workshops for peers and juniors.• Strong organizational and management skills with the ability to adapt to competing priorities and to manage multiple deliverables and challenging study requirements.• Good interpersonal and communication skills, fostering strong rapport with all stakeholders. Show less