Clinical Research Coordinator Public Health Sciences

Responsibilities

• Conducting participant visits in community and residential settings, obtaining informed consent, collecting blood samples, administering cognitive assessments, and gathering family and medical histories
• The coordinator also prepares and ships research specimens, participates in clinical classification meetings, and supports Institutional Review Board (IRB) submissions, regulatory compliance, and study documentation
• Assists in the administration and coordination of all phases of the assigned project as directed
• Responsible for ensuring that all aspects of the study are conducted following the study protocol
• Represents the project by serving as the study liaison and representative
• May guide other study personnel by providing training, direction, guidance, and evaluation of work activities
• Coordinates and participates in recruitment data collection, and follow-up activities
• Collect blood samples
• Must be able to travel to collaborating institutions and travel to homes of the participants local, state, and nationally
• Assists with the development of collection methods; creates and revises study materials, forms, manuals, and brochures as requested
• Assists with and provides reports as requested
• Provides guidance and/or performs data processing and coordinates data analysis; oversees quality assurance of data
• Orders and maintains adequate supplies for the project
• Initiate introductory visit following timeliness guidelines per study standards
• Actively participates in outreach/community education and/or early detection/screening events around AD
• Provide presentations around AD and other related dementias
• Performs other related duties incidental to the work described herein
• Under departmental direction, coordinates activities to support multiple research studies of all phases
• Serves as the principal administrative liaison for assigned studies with the ability to manage a workload that includes studies of increased complexity
• Develops and maintains recordkeeping systems and procedures to ensure compliance with study protocols and all appropriate regulations
• Attends clinic as needed to perform activities including, but not limited to: assist the research team with recruitment activities, administer questionnaires and answer any questions about future appointments
• Responsible for the compilation, registration and submission of data, as required by the Sponsor

Preferred

• A Bachelor's degree in public health, Basic Science, or a relevant clinical discipline
• a master's degree
• Phlebotomy license
• SOCRA or ACRP Certification

Benefits

• Premium pay such as shift, on call, and more based on a teammate's job
• Incentive pay for select positions
• Opportunity for annual increases based on performance
• Paid Time Off programs (eligibility may depend on your FTE or status)
• Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability (eligibility may depend on your FTE or status)
• Flexible Spending Accounts for eligible health care and dependent care expenses (eligibility may depend on your FTE or status)
• Family benefits such as adoption assistance and paid parental leave (eligibility may depend on your FTE or status)
• Defined contribution retirement plans with employer match and other financial wellness programs (eligibility may depend on your FTE or status)
• Educational Assistance Program (eligibility may depend on your FTE or status)
• Glassdoor
• 3.7
• Atrium Health Wake Forest Baptist is a nationally recognized academic medical center and health system based in Winston-Salem, NC, part of Advocate Health, the third-largest nonprofit health system in the United States.
• Winston Salem, North Carolina, USA
• https://www.wakehealth.edu
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Qualifications

• Experience in a medical and/or research setting
• Paramedical or other clinical experience
• One year of clinical and or survey research experience including interviewing, and supervision of data collection procedures
• An equivalent combination of education and experience will be considered
• Valid NC Driver's License
• Bachelor's degree with two years; experience in clinical research; or an equivalent combination of experience and education
• A Bachelor's degree in public health, Basic Science, or a relevant clinical discipline
• A master's degree
• Phlebotomy license
• Registered Record Administrator
• SOCRA or ACRP Certification
• One year of clinical and or survey research experience including interviewing, and supervision of data collection procedures.
• Bachelor's degree with two years; experience in clinical research; or an equivalent combination of experience and education.

Required skills

• ACRP Certification, CITI Human Subjects Research Certification, Clinical Research, Interviewing, North Carolina Driver’s License, Phlebotomy, Registered Record Administrator, SOCRA Certification, Survey Research

Preferred skills

• Phlebotomy license, SOCRA or ACRP Certification, a master's degree

Experience

• 2+ years