JOB SUMMARY

Under general supervision, develops, coordinates, and administers the logistical aspects of clinical trials according to good clinical practice (GCP), good documentation practices (GDP) and standard operating procedures (SOP). Acts as a pivotal point of contact and communication between department staff, clinical sites, as well as vendors.

KEY RESPONSIBILITIES

1. Oversee and manage operational aspects of clinical trials in conjunction with project teams and in accordance with SOPs, GCP, GDP and specific country regulations, and may prepare clinical trial budgets.
2. Collaborate and partner with a cross-functional team which includes clinical field, site managers, monitors, safety, and others.
3. Build and maintain optimal relationships and effective collaborations with various internal and external parties.
4. Develop, test, and implement clinical tools to provide relevant information for clinical studies management....