CRA/SCRA-Biosimilars (West Coast)

• This position is responsible for project management and study site management from site selection to initiation until monitoring and close‑out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonisation Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations;
• The position is responsible for ensuring that all data generated by the assigned sites is of high quality, on time and within budget.

Responsibilities

• Planning of project activities and study timelines based on project goal and sponsor's expectation;
• Organize and Lead meeting/teleconferences for study activities implementation (e.g. investigator meeting, project review meeting etc), monitoring the progress of each CRA responsible sites, and assessing overall status of the project;
• Develop the project management plan, moni...