Clinical Research Associate Resume New York, NY - Hire IT People

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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Clinical Research Associate Resume

New York, NY

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