AddressRequired Visa Status:
| Citizen | GC |
| US Citizen | Student Visa |
| H1B | CPT |
| OPT | H4 Spouse of H1B |
| GC Green Card |
Employment Type:
| Full Time | Part Time |
| Permanent | Independent - 1099 |
| Contract – W2 | C2H Independent |
| C2H W2 | Contract – Corp 2 Corp |
| Contract to Hire – Corp 2 Corp |
Description:
POSITION SUMMARY
Functions as the coordinator on various research studies. Coordinates all study procedures to identify and consent available subjects, consistent study procedures and techniques and verified documentation. Collects and maintains study samples. Position performs duties associated with data collection, management of data generated by study protocols, and assists with interpretation of data.
PREFERRED QUALIFICATIONS
- Clinical research certification.
- Working knowledge of techniques and methodologies used in developing, coordinating, and managing Clinical Research projects with working knowledge of database management spreadsheets, and software.
REQUIRED QUALIFICATIONS
- Bachelor’s degree.
- Minimum of two years of Clinical Research experience.
- A combination of relevant work and college education equaling six years may substitute for this requirement.
Responsibilities:
- Confers with PI to assist in developing plans for research projects and discuss the interpretation of results; collaborates in the preparation of manuscripts for publications and preparation of grant proposals to sponsoring agencies; assists in the preparation of amendments to protocols and/or modifications to study design as appropriate.
- Works with study monitors, as applicable, for data queries and site visits.
- Coordinates the development of forms, questionnaires, and the application of research techniques; assists in writing instructional procedure manuals for study progress, data collection and coding.
- Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; identifies problems and/or inconsistencies and monitors participant’s progress to include documentation and reporting of adverse events.
- Performs other duties incidental to the work described herein.
