Associate Clinical Research Specialist Jobs in Nevada

Knowledge of ICH and local regulatory authority regulations regarding drug

Experience in monitoring all trial components (PSSV to COV)

Ability to travel as needed (greater than 40%)

Strong organizational and time-management skills.

Collaborate with cross-functional teams to ensure the successful execution of clinical trials, including data management, biostatistics, and medical writing.

Perform site qualification, initiation, and close-out visits, including site selection, site initiation, and site closure.

Identify and escalate study issues to the appropriate stakeholders, including the clinical project manager, medical monitor, and regulatory affairs.

Minimum of 2 years of experience as a CRA in the biotechnology or pharmaceutical industry or academic space

Experience in oncology and solid tumors is required.