Summary
Overview
Work History
Education
Skills
Therapeutic Experience
Affiliations
System Vendor Experience
Timeline
Generic

Maggie Tasong

Bowie,MD

Summary

Clinical Research Associate with 5 years of clinical research experience with a Clinical Research Organization conducting trials from start up to close out following ICH and GCP guidelines. As a Clinical Research Associate, Maintained current regulatory documentation according to Essential Regulatory Document Guidelines and Trial Master File Plan. Maintained timely and effective communication amongst team members and site staff. Assumed responsibility for site management and site staff performance. Ensured that the Data clarification Form are accurate and are collected in a timely manner and assisted with the preparation of study start up materials and tools, as requested.

Overview

16
16
years of professional experience

Work History

Clinical Research Associate

Concentrics CRO
11.2019 - Current
  • Responds to site issues identified during monitoring visits (i.e., non-responsive site, Protocol Deviations concerns, and quality issues)
  • Obtains consents, signatures, and other required documentation
  • Performs documentation and monitoring of all clinical research trial data
  • Conducts protocol training to staff at investigator site(s) during site initiation visit, to ensure that site(s) is/are equipped to conduct the clinical study
  • Performs site visits which includes - site qualification, initiation, monitoring and close-out visits
  • Performs and coordinates assigned aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the safety and efficacy of investigational products and/or medical devices
  • Reviews protocol violations with investigators and implemented corrective actions to ensure future compliance with the protocol and applicable regulations (FDA/GCP/ICH/IRB)
  • Reviews investigator’s files to ensure that all documents are in order and ready for audit or inspection.

Study Coordinator

Grant Park Rehabilitation
Washington DC
09.2016 - 10.2019
  • Assured compliance with all aspects of individual studies
  • Ensured that protocol procedures had been completed accurately, safely, and in a timely manner
  • Performed research assessment and patient intervention under the supervision of the Principal Investigator (PI)
  • Ensured all relevant regulatory and Good Clinical Practice (GCP) guidelines are adhered to
  • Provided research coordination within the Clinical Trials Department and worked with the NHS
  • Ensured the timely coordination and completion of study related procedures within assigned responsibility
  • Participated in patient recruitment and enrollment, data collection, source documentation, quality assurance, drug accountability and review, regulatory submissions of events as needed, protocol dissemination to health care professionals.

Licensed Practical Nurse (Home Care)

Reliable Health Care Services
01.2010 - 08.2016
  • Provided care to pediatric and adult patients with compromised airway (tracheostomy tube, ventilators)
  • Managed gastroenterological issues such as (gastrostomy tube, and Nasogastric tube)
  • Medication administration of oral (PO), Intramuscular Injection (IM), Subcutaneous Injections and Inhalation Medications.

Geriatric Licensed Practical Nurse

Hebrew Home of Greater Washington
Rockville MD
06.2008 - 12.2009
  • Performed initial admission assessments
  • Made use of the nursing process to accurately assess, diagnose, plan, execute interventions, and evaluate results
  • Communicated effectively with patients, family, physicians, and other disciplines throughout the course of treatment
  • Administered medications (IV, IM, SQ, intradermal, and PO) as prescribed
  • Assessed patients’ status and promptly notify physician of any clinical changes
  • Performed clinical tasks according to facility protocol
  • Kept patient safety and confidentiality as primary focus of concern
  • Employed universal precautions in all patient interactions
  • Demonstrated solid teamwork skills, developed over four years of working as a member of a comprehensive team in a variety of clinical settings
  • Provided care that included pain management, insertion and maintenance of Foley catheters, wound care, G/J-tube care and supporting patients in Activities of Daily Living (ADL).

Education

Clinical Research

Clinical Research Training
Scottsdale, AZ
02-2019

Nursing Diploma -

Radians College
Washington, DC
05-2008

Associate of Science - Nursing

Meridian Global University
Greenbelt, MD

Skills

  • Project Management
  • Detailed documentation
  • Research and Development
  • Clinical Documentation
  • Data Collection
  • Report Writing

Therapeutic Experience

  • Neurology/CNS, Parkinson Disease, ALS, Dementia, Phase II, Phase III
  • Gastroenterology, Chron’s Disease, Ulcerative Colitis, Phase IV
  • Rheumatology, Rheumatoid Arthritis, Axial Spondylarthritis, Psoriatic Arthritis, Phase IV
  • Psychiatry, Bipolar Disorder I, Phase IV
  • Infectious Disease, Covid -19, Phase II, Phase III

Affiliations

  • CITI Program – GCP/ICH
  • Maryland LPN license # LP44975
  • American Heart Association CPR Certification, BLS

System Vendor Experience

IBM Clinical, Inform, iMedidata, Siebel Clinical, Suvoda, Almac, Veeva Vault, Epic

Timeline

Clinical Research Associate

Concentrics CRO
11.2019 - Current

Study Coordinator

Grant Park Rehabilitation
09.2016 - 10.2019

Licensed Practical Nurse (Home Care)

Reliable Health Care Services
01.2010 - 08.2016

Geriatric Licensed Practical Nurse

Hebrew Home of Greater Washington
06.2008 - 12.2009

Clinical Research

Clinical Research Training

Nursing Diploma -

Radians College

Associate of Science - Nursing

Meridian Global University

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Maggie Tasong