We provide IT Staff Augmentation Services!

Health Care Documentation Specialist Resume

AREAS OF EXPERTISE:

SDLC - Agile and Waterfall

CSV Framework

Healthcare Documentation

Clinical Trial Process

ICH GCP

Pharmacovigilance

Spectroscopy & Chromatography

HIPAA

Medical Billing

Information Assurance

Clinical Data Management

Clinical Pharmacology

SOFTWARE SKILLS:

HP ALM, JIRA, MS Project, MS Visio, MS Office, Synapp, SQL Digital Asset Management Products: Nuxeo, OpenText Media Manager, Veeva Vault

PROFESSIONAL EXPERIENCE:

Confidential

Health Care Documentation Specialist

Responsibilities:

  • Processed 100 daily average medical claims including bulk billing, no-gap, known-gap, full gap, third-party claims, inpatient and outpatient using Synapp web application.
  • Resolved medical billing discrepancies by collaborating with health funds, insurance organizations and Medicare representatives
  • Improved operational compliance of medical billing by enabling the registration of medical providers with health funds
  • Documented Standard Operating Protocols (SOPs) for the medical billing process; Trained new team members for project onboarding

Confidential

Clinical Research Associate

Responsibilities:

  • Quality checked (QC) Adverse Event (AE) reports, investigator brochures, clinical study reports, and trial master files in clinical trials
  • Collaborated with CPL, CRAs, Pharmacologists, and Investigators to perform QC and manage regulatory documents
  • Trained on protocols for Site Selection Visit (SSV), Site Initiation Visit (SIV), Interim Monitoring Visit (IMV) and Close Out Visit (COV)
  • Ensured compliance with SOPs, GCPs, ICH guidelines, cGMP regulations related to CSV that includes 21 CFR part 11, 210 & 211
  • Created a Clinical Study Report (CSR) with medical writer; Included SAS based reports working with biostatisticians during clinical trials

Confidential

Research Intern

Responsibilities:

  • Studied industrial training for one month which included 15 days in manufacturing and 15 days in analytical lab
  • Collaborated with cross-functional specialists such as research analyst, quality control team to learn drug manufacturing process

Hire Now