Senior Medical Assistant

Senior Medical Assistant

Secaucus, NJ

Duties: Responsible for working under the guidance of the Principal Investigator and Sub-Investigators; Director, Associate Director, CRC Clinical Operations; Manager, Clinical Operations; Senior Clinical Research Coordinators, and Clinical Research Coordinators to perform study procedures required in clinical
studies conducted on behalf of sponsors at the Frontage Clinical Services.

Supervises: None

Qualifications: Associate or Bachelors degree in a biomedical discipline or related scientific discipline or
equivalent experience. Good communication skills with the ability to interact with the Principal Investigator, Sub-Investigators, and Frontage Clinical Services and sponsor personnel. Completion and certification of Medical Assistant course from an accredited or allied health training school.

Experience: Three (3) year experience in clinical research is desirable. Knowledge of FDA regulatory requirements is necessary or on job mandatory training will be required.

Specific Responsibilities:
· Assist Clinical Study Coordinators in any task as needed.
· Develop a high level of familiarity and knowledge of the study protocol and flow chart of study procedures. Develop a strategy for implementing study procedures in compliance with study protocols.
· Labeling, taping (e.g., sample collection and transfer tubes, safety labs, urine cups, etc.)
· Blood donation procedures (e.g., hemopoint calibration, source document preparation).
· Assist Clinical Research Coordinator in transcribing study data from source documents to sponsor
designated case report forms or records data for remote data entry is applicable.
· Perform study procedures (e.g., venipunctures, obtain and process biological specimen samples, vital signs, safety assessments, etc.) as required by study protocol under the supervision of the Principal Investigator and Sub-Investigators; Director, Associate Director, CRC Clinical Operations; Manager,Clinical Operations; Senior Clinical Research Coordinators; and Clinical Research Coordinators.
· Perform duties of Clinical Research Coordinator under the supervision of the Principal Investigator and Sub-Investigators; Director, CRC Clinical Operations; Manager, Clinical Operations; Senior
Clinical Research Coordinators; and Clinical Research Coordinators.
· Record study data in the source documents. Evaluate and review study data to ensure accuracy and completeness.
· Assist in managing training records as needed.

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