Sort by
Refine Your Search
-
Coordinate and execute stage setups and strikes, including music stands, chairs, risers, pianos, percussion instruments, microphones, and related performance equipment. Transport, position, and prepare
-
with study documentation, protocol submissions, and standard operating procedures (SOPs). Is responsible for all aspects of managing and documenting Investigational Product (IP); including arrival
-
(MTAs, CDAs, DUAs, DTAs, etc.) are necessary and alerts appropriate parties. Prepares FDA regulatory submissions in collaboration with ORAQ, including development, submission, and maintenance of relevant
-
, documentation, and analysis of clinical research data. May oversee the work of junior staff and train or mentor others in clinical research tasks. Be Bold. Research Operations Recognizes when typical agreements
-
train Clinical Research Specialists (CRSs) in these tasks. Work Performed Research Operations Under supervision, assists with managing investigational products (IP) including arrival, storage, and
-
with study level documentation and approvals for international studies. Under supervision, assists with managing investigational products (IP) including arrival, storage, and handling (requisitions
-
research data and may train Clinical Research Specialists (CRSs) in these tasks. Operations: Under supervision, assists with managing investigational products (IP) including arrival, storage, and handling
-
: Recognizes when typical agreements (MTAs, CDAs, DUAs, DTAs, etc.) are necessary and alerts appropriate parties. Prepares FDA regulatory submissions in collaboration with ORAQ, including development, submission
-
of managing and documenting Investigational Product (IP); including arrival, storage, tracking, and provision to research participants. Prepares for and provides support for study monitoring and audit visits
-
operations of a clinical research team conducting multiple, complex oncology clinical trials, including studies involving Investigational Products (IP). You will partner closely with Principal Investigators