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Clinical Research Associate Resume

New York, NY

SUMMARY:

Clinical Research Associate with multiple therapeutic experience and a strong electronic data capture background looking for a position as a site monitor with a clinical research organization, biotechnological or pharmaceutical company.

SKILLS:

Cardiovascular, Biomedical Devices, Oncology, CNS, Infectious diseases, and respiratory.

PROFESSIONAL EXPERIENCE:

Clinical Research Associate

Confidential, New York, NY

Responsibilities:

  • Monitors and co - monitors clinical studies to ensure data quality and integrity
  • Ensures adequate investigational drug supplies are maintained at the site based upon enrollment demands
  • Conducts ongoing review of regulatory document files
  • Participates in the review of clinical protocols and provides input
  • Managed case report forms (CRF) and clinical data flow
  • Assisted with project meeting organization
  • Participated in data management processes including the collection and cleaning of data, and the identification and resolution of data queries
  • Perform drug reconcilation
  • Documents and distributes visit findings in trip reports.

Public Health Consultant

Confidential

Responsibilities:

  • Plan and execute public health awareness programs
  • Conduct meetings and forums with multi disciplinary medical and mental health professionals
  • Visit and report on government healthcare establishments
  • Monitor and evaluate patient admit procedure and general policies
  • Advise on quality improvement recommendations

Clinical Research Associate

Confidential, Cupertino, CA

Responsibilities:

  • Conduct pre-study, initiation, interim monitoring and close-out visits
  • Implements, monitors and reports clinical trials in conformity with Confidential / Confidential and other local regulations
  • Providing a leadership role in completing project activities associated with monitoring functions of Phase II-IV clinical research studies
  • Performing CRA and investigator site management activities in adherence to all applicable regulatory guidelines and standard operating procedures (SOPs)
  • Create and properly files trip reports, follow-up letters and telephone contacts for assigned investigative sites
  • Evaluate and Resolve Data Queries
  • Evaluate study query trends and interacts with Study Team in improving data quality
  • Assist investigative sites with timely and accurate resolution of queries
  • Attend and participate at Investigator Meetings

Emergency Medical Technician

Confidential, NY

Responsibilities:

  • Assist in stabilizing emergency medical patients
  • Monitoring, documenting client vitals, intakes, outputs, and abnormal findings.
  • Communicating with nurses, doctors and other health care staff
  • Medical/ surgical patients, Psych Unit, ER, CPEP

Clinical Nurse Associate

Confidential, Philadelphia, PA

Responsibilities:

  • Chart and document patient vitals, chest tubes, fluids and blood sugar levels
  • Plan and implement patient safety protocols to decrease injury
  • Educate peers of new skills and standards
  • Member of RAPID RESPONSE TEAM
  • Medical/ surgical patients, THORACIC ONCOLOGY

Clinical Assistant

Confidential, Allentown, PA

Responsibilities:

  • Provide client centered social and emotional support
  • Assist patient with daily activities while maintaining patients highest level of independence
  • Communicate with other medical professionals on client’s needs and progress

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