Start Date
Immediate
Expiry Date
09 Nov, 25
Salary
0.0
Posted On
10 Aug, 25
Experience
0 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Documentation, Professional Manner, Immunity, Variance Analysis
Industry
Pharmaceuticals
JOB SUMMARY:
Responsible for managing many aspects of conducting clinical trials, projects, consenting collections, and testing for research clients both from internal (hospital based, Medical Director- Researchers) and external clients. Serves as central coordinator of study activity at the research site, acting as liaison between the investigator and all internal and external contacts. Responsible for a variety of complex tasks requiring independent judgment regarding the pre-implementation and implementation phases of a study, such as feasibility discussions, contract and budget preparation, study startup activities, subject recruitment and enrollment, maintenance of the study, data management, and study closure. Participate as effective team member in section management relative to communications and operations as appropriate.
MINIMUM EDUCATION:
MINIMUM EXPERIENCE:
IMMUNIZATION REQUIREMENTS:
Prove Immunity to Hepatitis B, be immunized, or sign a waiver refusing Hepatitis immunization. Provide documentation of a PPD test conducted not more than 90 days prior to date of hire or have a PPD test conducted through TriCore.
GENERAL REQUIREMENTS:
Please refer the Job description for details