Sheridan Eiman Email & Phone Number

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.

South Africa

● 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

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

Pretoria, Gauteng, South Africa

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.

Pretoria, South Africa

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