Coord, Research
About The Position
The Department of Dermatology is seeking a Research Coordinator with exceptional verbal and written communication skills to join a diverse team of clinical investigators. This position supports and augments the investigators in the conduct of dermatology clinical trials recruiting subjects for a variety of research on topics. The successful applicant would recruit and coordinate research subject enrollment and investigational product administration, follow-up and data entry, compile and report safety information as needed to the local IRB, sponsors and regulatory agencies and maintain the investigator site files.
Requirements
- Bachelor's degree; at least 1 year of experience directly related to the duties and responsibilities specified.
- Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis.
Nice To Haves
- Experience in using Electronic Data Capture/Collection (EDC) software (REDCap, Medidata, Firecrest, Signant Health etc.)
- Experience working with Protected Health Information (PHI)
- Experience in identifying and recruiting research subjects
- Very strong verbal and written communication skills
- Microsoft Office products including spreadsheets (Word, PowerPoint, Excel)
- Delivering oral presentations to small groups
- Experience with preparation and submission of IRB documents for review and approval
- Experience with ClickEra or other eResearch portals
- Experience with hands-on patient care (vital sign collection, phlebotomy, centrifuge)
Responsibilities
- Screen and recruits subjects and coordinates follow-up activities to meet aggressive enrollment targets; collects, processes, and assists in the compilation and verification of research data, sample, and/or specimens, following strict protocol and detailed instructions.
- Conducts and records face-to-face and/or telephone interview with subjects, in accordance with predetermined interview protocol, data collection procedures, and documentation standards.
- Coordinates nurses, pharmacists and technical staff in the completion of protocol requirements and maintain enrollment documentation adequate to demonstrate protocol adherence
- Maintains the study related documentation in the investigator site file in compliance with federal regulatory guidelines
- Performs data analysis and interpretation, as specifically assigned; may utilize specialized analytical equipment and/or instrumentation, or specified statistical data analysis programs software.
- Organizes clinical in-service trainings, investigational team meetings and informational sessions to support study adherence; coordinates research equipment setup, operation, and maintenance
- Communicates with internal stakeholders, sponsors and regulatory agencies (ie IRB) as needed to facilitate study activities and participates in regular departmental and study team meetings to report of study progress and deliverables.
Benefits
- medical, dental, vision, and life insurance
- educational benefits through the tuition remission and dependent education programs
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
