Kenneth Granville

Research Program Manager

Columbia, MD 21044

ad17ws@r.postjobfree.com

+1-410-***-****

Work Experience

Clinical Data Manager

Actalent - Richmond, VA

September 2020 to October 2022

Maintained clinical and regulatory documents for subjects and site via electronic data capture platforms Reseach Coordinator

Washington health Institute - Washington, DC

September 2019 to March 2020

Enrollment of trial participants and coordinating all aspects of a practice based research program Research Program Manager

Capital Medical Associates - Washington, DC

2010 to 2018

See resume

Research Coordinator

CRM Dermatology - Baltimore, MD

2008 to 2011

Clinical Trials Manager

Algorithme Pharma - Baltimore, MD

2008 to 2009

QA Consultant

Quality Associates, Inc - Columbia, MD

2006 to 2008

Clinical Research Coordinator

Woodholme Gastroenterology Associates - Pikesville, MD 2005 to 2006

Clinical Research Associate

Suburban Hospital Cancer Program - Bethesda, MD

2003 to 2005

Clinical Research Specialist/ Pharmacy Technician

Washington Oncology Hematology Center - Washington, DC 2000 to 2002

Education

Associates of Science in Hospital Administration

University of South Carolina

Certificate of Pharmacy Technique in Pharmacology

Naval School of Health Sciences

Skills

• GCP

• CLINICAL TRIAL

• DATABASE

• EMR

• EXCEL

• Program Management

• Clinical Research

• Pharmacy Technician Experience

• Research

• Laboratory Experience

• Hospital Experience

• Data Collection

• CRM Software

• Epic (2 years)

• FDA Regulations

• Microsoft Excel

• Primary care

• English

• Communication skills

• Clinical trials

• Organizational skills

• EKG

• Phlebotomy

• Vital signs

• Medical records

• Anatomy knowledge

• Medical Terminology

• Databases

Certifications and Licenses

Pharmacy Technician License

Additional Information

CCRC certified professional offering 18+ years of experience in clinical research coordination enrolling over 500 subjects successfully in pre-clinical thru phase IV research studies with a demonstrated ability to

support the management and coordinate the tasks of multiple clinical research studies. Expert in liaising

with different departments. Special talent for creating and maintaining databases and reports. KNOWLEDGE, SKILLS, & ABILITIES

• Working knowledge of medical and research terminology.

• Working knowledge of federal regulations for human subject protections and Good Clinical Practices (GCP).

• Ability to communicate and to work effectively with a diverse team of professionals.

• Excellent organizational and prioritizing capabilities

• Strong computer skills with demonstrated abilities using clinical trial database, electronic data capture, and MS Word or Excel.

(Nextgen and Epic EMR), Medidata, Clinphone-Perceptive, OpenClinica, Inform, Quintiles Infosario

• Excellent interpersonal skills, detailed-oriented, and meticulous.

• Excellent professional writing and communication skills.

• Ability to work independently in a fast pace environment with minimal supervision.

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