Start Date
Immediate
Expiry Date
29 Nov, 25
Salary
0.0
Posted On
30 Aug, 25
Experience
0 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Good communication skills
Industry
Hospital/Health Care
BENEFITS AT A GLANCE
Under direct supervision, this position will be responsible for supporting Principal Investigator(s), clinical research coordinators, and other more senior members of a clinical study team with administrative, regulatory, and data management tasks as assigned. Key tasks may include: case-finding, evaluation and abstraction of source documentation, case report form completion, database use and management (including our institutional CTMS), data abstraction and organization for presentation/publications. Responsible for subject data management and maintaining source documents and subject files according to Good Clinical Practice. May assist with preparing and shipping medical samples/specimens to/from appropriate labs, providing administrative support to study activation processes and regulatory maintenance of assigned studies.
The CDM Floater will be dedicated to the Massey Clinical Trials Office. The CDM Floater works closely with the Assistant Director of Clinical Research Operations and Workforce Development to support continuing data entry clean up and compliance for all studies across disease working groups. The CDM Floater will also function as a Patient Pre-Screener to assist teams in identifying potential study candidates. This role accommodates flexible work arrangements but does expect monthly in person meetings and additional trips on site as needed.
Each agency within the Commonwealth of Virginia is dedicated to recruiting, supporting, and maintaining a competent and diverse work force. Equal Opportunity Employer