Experience

TASK Eden

• South Africa
• Research Services
• 1 - 100 Employee

• Lead Site Administrator

  • Aug 2022 - Present

• Clinical Trial Administrator

  • Mar 2021 - Aug 2022


Department of Social Development
• Government Relations
• 700 & Above Employee
• Administrative Clerk

  • Nov 2017 - Jan 2022

PathCare
• South Africa
• Medical Practices
• 700 & Above Employee
• Helpdesk

  • Jun 2016 - Oct 2017


Quintiles

• Spain

• Proposal Developer 2

  • May 2015 - Dec 2015

  •Review Requests For Proposal (RFP). •Identify information for proposal text and budget development; and work closelywith proposal development team to prepare and finalise proposals• Prepare text and budget for proposals, rebids and related documents• Provide support and assistance to other Proposal Developers in the delivery of assigned opportunities• Team Lead on assigned projects, to develop proposals and budgets• Participate in strategy calls to discuss customer requirements and identify discrepancies in customer information• Perform quality control edits on all documents and participate in the finalization of documents and distribution to thecustomer and internal departments• Update and maintain corporate databases as required and ensure accurate information is included in tracking reports• May participate in training / coaching / mentoring new staff• May participate in customer meetings• Perform all other duties as assigned Show less

• Senior Clinical Trial Assistant

  • Oct 2014 - Apr 2015

  Assist Clinical Research Specialist (CRS)/In-house Clinical Research Specialist (iCRS), Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.Collaborate with Clinical Project Manager (CPM), CRS/iCRS, CRAs/iCRAs and RSU on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files and completeness.Collaborate with CRS/iCRS, CRAs/iCRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.Assist in training and orienting new staff. May act as a mentor for less experienced CTAs.May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval.Perform assigned administrative tasks to support team members with clinical trial execution. Show less

• Clinical Trial Assistant

  • Jan 2012 - Sep 2014

  Assist Clinical Team Lead (CTL) and Clinical Research Associates (CRAs) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for accuracy and completeness.



Parexel International

• Team Leader

  • Jan 2009 - Nov 2011

  Lead, train and direct the Clinical Trial Assistants and to assist clinical with the preparation and execution of trials Lead, train and direct the Clinical Trial Assistants and to assist clinical with the preparation and execution of trials



PAREXEL

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Quality Management Assistant

  • Jan 2008 - Dec 2008

  Assist with and/or organize/schedule meetings/audits/inspections etc., as well as subsequent requirements thereof. SOP/management system administration & maintenance; update and maintenance of PAREXEL George performance and compliance information.

• Clinical Trial Assistant

  • Mar 2006 - Dec 2007

  Complete any administrative responsibility that the Clinical Team Leader or Study Coordinator may delegate, within the conduct of a specific trial. Prepare and maintain the necessary files and essential documents for a specific clinical trial. Liaises with laboratories concerning the transcription of demographic and study information on laboratory reports