Sheridan Eiman

Experience

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  Institut d'Expertis Clinique Afrique du Sud

  Feb 2010 - Aug 2012

  Technical and Scientific Officer
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  Future Cosmetics CC

  Sept 2012 - Apr 2018

  Senior Technical and Scientific Manager

  In this role he broadened his experience by gaining business and leadership skills. Successfully increased company profit margins, reduced staff turnover, increased team output and successful trial executions and delivery.Key responsibilities included: Clinical trial coordination, Manufacturing operations, Quality Management Systems, Product safety and efficacy testing, General Lab and Factory Operations, Stakeholder management and budget control. Regulatory compliance and submissions

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  Freelance

  Oct 2018 - now

  Clinical Trial Support

  ● Raw data compilation● Data Analysis● Clinical Trial report writing● Independent Review Board (IRB) applications and submissions – Ethics clearance and approvals● Regulatory submissions● Customer representation in South Africa

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  British High Commission Pretoria

  May 2019 - Dec 2019

  Science and Innovation Officer

  Promote and advance the UK offer in Science, Technology and Innovation. In short space of time, successfully built linkages, relationships and networks for UK stakeholders with delivery partners in SA governmental and private sectors, across industries. Project initiation and monitoring of Science and Innovation projects of UK government in South Africa. Stakeholder management, strategy development and implementation.

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  Human Science Research Council (HSRC)

  Feb 2021 - Nov 2021

  Clinical Trial Project Manager

  Direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. Plan, direct, or coordinate clinical research projects. May also evaluate and analyse clinical data

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  WCG ThreeWire

  Sept 2021 - now

  Country Manager

  Present WCG Frankfurt GmbH services to local CRAs and sponsors. • Host conference calls discussing WCG Frankfurt GmbH services with Study Site Team. • Reach out to Study Site Investigators and Study Site Team to assess Sites’ needs and identify opportunities to provide/sell WCG Frankfurt GmbH services. • Assist with contracting requirements with medical institutions. • Select and provide training of study personal and Clinical Research Coordinators. • Manage of study personal, Clinical Research Coordinators and referral and community outreach programs. • Follow-up with Study Site Team regarding current initiatives and offer alternative services/solutions where applicable. • Provide overall support to ensure program success (weekly client and site updates). • Report program results to Program Managers. • Manage invoicing approvals • Update Site Status Tracker and reporting program results to Program Manager. • Assist in presenting status reports to clients/sites and WCG Frankfurt GmbH management. Show less