Job Description

Certification Details

• BLS - Basic Life Support
• State License 1 Verification

Job Details

• Required:
• * Associates Degree
• * 3 years of Clinical Research Experience
• * BLS
• Preferred:
• * Bachelors Degree
• * SoCRA or ACRP Certification
• * Phlebotomy Certified
• * Medical Assistant Diploma
• * Experience with Oncology setting
• Primary Duties and Responsibilities
• * Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety.
• * Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE’s and source documents.
• * Responsible for screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed consent process.
• * Responsible for accurate and timely data collection, documentation, entry and reporting, including resolution of queries from sponsors or regulatory entities.
• * Coordinates institutional, pharmaceutical and internal audits, including facilitating third party study monitoring and designs and implements needed corrective actions.
• * Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
• * Responsible for timely submission of adverse events, serious adverse events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
• * Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality.
• * Plans and coordinates strategies for increasing research participant enrollment, and/or improving clinical research efficiency as needed.
• * Provides technical support for the preparation of grant proposals, publications, presentations and special projects.
• * Provides assistance with research project budget development, including identifying and classifying routine care vs. research related care and provides assistance with research participant research billing and reconciliation.
• * Attend meetings and conferences related to research activities, including research staff meetings.
• * Participate in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as necessary or requested; Participates in training and education of new research personnel.

Job Requirements

• Required Certifications:
• * BLS - Basic Life Support
• * State License 1 Verification

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