CHARLENE CASH

WINSTON- SALEM, NC *****

adupf2@r.postjobfree.com

336-***-****

PROFESSIONAL EXPERIENCE

June 2021 -Present ASSOCIATE PROJECT MANAGER – WORLDWIDE CLINICAL TRIALS _ (Homebased)

• Lead core project team and facilitate their ability to lead extended/complete project team assignment’s• Lead cross unit coordination both internal and external, inclusive of subcontractor • Define and manage project resource needs and establish contingency plans for key resources • Ensure successful design, implementation, tracking and revision of project plans for assigned projects • Promote effective teamwork among project team members Resolve conflicts as needed • Ensure appropriate communication on project-related matters with the PM Management • Meet financial performance targets for the assigned clinical projects · Ensure project deliverables are met according to both WCT and client expectations • Can be key client contact for assigned projects • Establish excellent working relationships with client project teams to ensure client satisfaction and operational excellence. • Ensure that all staff allocated to assigned projects adheres to professional standards and SOPs established for clinical research. • Manage all aspects of designated projects • Perform other duties as assigned by team and/or management.

March 2017 TO May

2021

ASSISTANT PROJECT MANAGER - INTERNAL MEDICINE/GERONTOLOGY/ NEUROSURGERY WAKE FOREST BAPTIST HEALTH

Overall study management to include initial start-up reviewing study applications thru study sponsored or in-house protocols, coordinating participants overall study experience and from the screening process thru to randomization until end of term. • Medical record review, and recruitment of patient population • Coordination of patients' study visits to include the entire process • Coordination, collection, and creation of site CRF’s per sponsor guidelines • EDC data entry & processing, AE & SAE reporting thru sponsored specific data bases. • Pre-analysis of data entered EDC data base for final analysis per the • Regulatory documents to include continuing reviews, protocol deviation reporting • Processed project payments thru Clincierge & CLIN card- Green spire.

NOVEMBER 2016 TO

OCTOBER 2015

Clinical Research Coordinator - Device Studies (Total Hip & Knee Replacement) Ortho Carolina- David Pollock, MD

CHARLENE CASH

WINSTON- SALEM, NC 27127

adupf2@r.postjobfree.com

336-***-****

Regulatory affairs coordinator with the local IRB, initial study applications, consent Form, CRF formation per sponsor request etc. • Screening and recruitment patient population • Coordination of patient study visits • Coordination, collection, and processing of data • Data processing & entry to EDC • Pre-analysis of data entered Excel for final analysis by the PI & Sponsor OCTOBER 2015 TO JANUARY 2006 Clinical Research Coordinator - Device Studies (Total Hip & Knee Replacement) Orthopedic Specialist of the Carolinas- David Pollock, MD Responsibilities • Regulatory affairs coordinator with the local IRB, initial study applications, consent Form, CRF formation per sponsor request etc. • Screening and recruitment patient population • Coordination of in person patient study visits • Coordination, collected and processing of data • Data processing & entry to EDC analysis of data processed thru Excel for final analysis by the PI OCTOBER 2015 TO

JANUARY 2006

Clinical Research Coordinator - Device Studies (Total Hip & Knee Replacement) Orthopedic Specialist of the Carolinas- David Pollock, MD

• Regulatory affairs coordinator with the local IRB, initial study applications, consent Form, CRF formation per sponsor request etc. • Screening and recruitment patient population • Coordination of in person patient study visits • Coordination, collected and processing of data • Data processing & entry to EDC • Pre-analysis of data processed thru Excel for final analysis by the PI

JUNE 2003 TO

NOVEMBER 2005

Clinical Research Coordinator/Data Collector- Neurorehabilitation Neurology WAKE FOREST BAPTIST HEALTH

• Regulatory affairs Coordinator • Screening and recruitment patient population • Coordination of patient's study visits • Coordination, collected and processing of data • Data processing & entry into the ED JUNE 2003 TO JUNE

2000

Research Specialist II WAKE FOREST BAPTIST HEALTH

• Screening and recruitment of stroke patients per study protocol • Coordination of study participants • Data processing and collection of data • Maintenance of data base system

CHARLENE CASH

WINSTON- SALEM, NC 27127

adupf2@r.postjobfree.com

336-***-****

EXPERTISE

Phases 1,2,3,4

THERAPEUTIC Areas Alzheimer’s Disease - Intervention & Device, Orthopedic -Total Hip & Knee Neurorehabilitation – Stroke, Cardiovascular

EDUCATION WINSTON-SALEM STATE UNIVERSITY

WINSTON-SALEM, NC BIOLOGY /CHEMISTRY