In this role, you will be responsible for supporting various projects within Environmental Branch (e.g., Phase I Environmental Site Assessments, asbestos sampling, compliance audits, NEPA projects, and wetland delineations) .
In this role, you will participate in the ongoing informed consent process, ensuring that human subjects, their families, and other health care providers clearly understand what is expected of and from them in the course of participating in a clinical/translational trial.
In this role, you will be responsible for supporting new product registration in terms of chemistry, manufacturing and controls requirements per the current regulatory environment and providing input to successful life cycle management of marketed assets.
In this role, the selected candidate will perform packaging and ships study specimens (blood, urine, etc.) to the sponsor or laboratory in accordance with sponsor and shipping guidelines and regulations, maintaining appropriate documentation.
In this role, the selected candidate will manage screening, consent volunteers, maintains accurate and timely documentation and communication with volunteers, research nurse and investigators, participants, IRB and other research related entities.
In this role, you will conduct background research and literature reviews to support primary research and analysis. The selected candidate will integrate data by linking clinical data to bench results and bioinformatics data output.
In this role, the selected candidate will provide, under direct supervision, support for specified research projects; collect, assess, and communicate data/results; assist in general laboratory operation and inventory.