LVN / Clinical Research Associate III, Vaccine Clinical Trials

3 weeks ago


Alhambra, United States HealthEcareers - Client Full time
Job Summary:
Manages day-to-day activities of a major segment(s) of medium to large studies or several smaller studies. May supervise project staff. Works under general supervision. Final review required for some phases of projects.
Essential Responsibilities:

    • Manages day-to-day activities of a major segment(s) of medium to large studies or several smaller studies.

    • May assist in development of study tools (e.g. tracking forms, questionnaires, chart review forms, etc.).

    • Develops simple study protocols or portions of complex protocols.

    • Monitors progress of study activities (e.g. data collection and validation, recruitment, pilot studies, focus groups, etc.).

    • May coordinate research project activities with other research study centers.

    • Prepares progress reports independently and/or collaboratively.

    • May participate in the training of new team members and/or clinical staff.

    • If assigned to clinical trial, may work with Sponsors/ monitors at clinical sites.

    • Adheres to compliance and privacy/confidentiality requirements and standards.

    • Adheres to GCP and compliance regulations for clinical trials.

    • Assists with and/or oversees quality assurance of study activities; ensures quality data.

    • May assist with implementation of quality control measures.

    • Acquires and maintains knowledge of KP systems and databases.

    • Identifies, recommends and implements solutions to study issues.

    • Interfaces with IRB and drafts portions of IRB protocols, amendments, continuing reviews, etc.

    • Supervises and manages the day-to-day activities of project staff including evaluating performance.

    • May mentor and develop staff and participate in hiring.

    • Contributes to portions of study presentations.

    • Assists in writing scientific articles.

    • Serves as a member on department or study-related committees.

    • May recommend budget actions/decisions and manage project budget.

    • Reviews scientific literature and drafts portions of background section of grant proposals.

  • May contribute to other sections of grants.

Basic Qualifications:
Experience

    • Minimum four (4) years of experience in public health, healthcare administration, epidemiology, or healthcare-related field.

    • Minimum two (2) years of training and/or professional experience in research methodology/research study design, hypothesis testing; OR

    • Minimum two (2) years of experience in clinical protocols involving research methodology/research study design, and hypothesis testing.

    • Minimum two (2) years of training and/or experience managing research projects under general guidance.


Education

    • Bachelors degree in public health, healthcare administration, epidemiology, or health-related field (ex. Biology, Psychology, etc.), OR four (4) years of experience in a directly related field.

    • High School Diploma or General Education Development (GED) required.


License, Certification, Registration

    • N/A


Additional Requirements:

    • Experience creating flow charts, research instruments (e.g. chart review forms, questionnaires, etc.).

    • Experience in quantitative and/or qualitative data interpretation and application.

    • Must be able to prepare sections of professional reports and presentations.

    • Must be able to work in a Labor/Management Partnership environment.


Preferred Qualifications:

    • Minimum one (1) year of direct personnel management preferred.

    • Masters degree in public health, healthcare administration, epidemiology or related field.

    • Preferred Qualification - LVN (Licensed Vocational Nurse)

    • Vaccine / COVID 19 Clinical Trials experience


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