
Asher Theoplus S
Research Associate

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Skills
Adverse Event ReportingAnalytical SkillsAnalyticsArtifactsBuild Strong RelationshipsClinical OperationsClinical Research ExperienceClinical Study ManagementClinical Trial Management System (CTMS)Contract Research Organization (CRO)DashboardsData AnalysisData ManipulationDefining RequirementsDevelopment OperationsDocument ProcessingDocument ReviewElectronic Trial Master File (eTMF)EnglishFeasibility StudiesGood Clinical Practice (GCP)ICHInstitutional Review Board (IRB)InvestigationKey Performance IndicatorsKOLLife SciencesManagementMicrosoft ExcelMicrosoft OfficeModeling ToolsMolecular BiologyMV REPORTOperational PlanningOral CommunicationProblem SolvingProject ManagementProtocolQuestionnairesRegulatory ExaminationsRegulatory RequirementsSDTMSite AcquisitionSite IdentificationSite ManagementStandard Operating Procedure (SOP)TMFTrackerVeevaVisualizationAbout me
As a Feasibility Manager at ICON plc, I leverage my expertise in clinical planning and trial management to support the successful execution of clinical trials. I provide strategic input to both internal and external clients, acting as a technical expert in feasibility processes.
Education

Karunya Institute of Technology and Sciences
2013 - 2017B. Tech Biotechnology
Experience

Par Pharmaceutical
Jul 2017 - May 2018Research Associate
ICON Central Laboratories
Jun 2018 - Apr 2020Site Services Specialist 1
PPD
Apr 2020 - Jul 2021Clinical Trial Coordinator II
IQVIA
Jul 2021 - Sept 2024TMF SME for Novartis.
CLINICAL PLANNING ANALYST 2
Dec 2022 - Sept 2024Senior TMF ANALYST
Jul 2021 - Dec 2022

ICON plc
Sept 2024 - nowFeasibility Manager
Licenses & Certifications

Medidata Classic RAVE EDC essentials for clinical research associte (monitors)
Medidata SolutionsJun 2021
Conversion tool for SAS
StatsMetrika Services Private Limited
Rave Reporter
Medidata SolutionsJun 2020
Rave query management
Medidata SolutionsJun 2021
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