Global Clinical Trial Coordinator

Predicine; Hayward, Northern (CA, KY); Hybrid; USD 70,000 - 95,000; Full time

Job summary

Predicine, located in Hayward, CA, is seeking a Clinical Trial Associate to support the planning, execution, and operational management of global clinical trials, working with cross-functional teams, sites, investigators, CROs and sponsors to ensure studies are conducted efficiently and in compliance with GCP and company procedures.

The ideal candidate is highly organized, detail-oriented, proactive, and able to manage multiple priorities in a fast-paced environment, with excellent communication

Qualifications

• Minimum 2 years of experience supporting clinical trials.
• Meticulous approach to documentation and study records.
• Experience supporting global clinical trials.
• Experience managing CROs and other clinical vendors.
• Familiarity with GCP, GCLP, ICH guidelines and FDA regulations.
• Ability to manage multiple priorities and timelines.

Responsibilities

• Support planning, coordination and day-to-day management of global trials from start-up through close-out.
• Manage timelines, milestones, deliverables and site enrollment tracking.
• Maintain communication with sites, investigators, sponsors and vendors.
• Support eTMF management and documentation control.
• Ensure compliance with quality, regulatory and audit requirements.
• Assist with data management, tracking data queries and issue resolution.
• Coordinate study meetings, prepare agendas and minutes.

Skills

Attention to detail

Organizational skills

Excellent communication

Collaboration

Problem solving

Education

Bachelor's degree in biology or life sciences

Advanced degree / CCRP / CCRA a plus

Tools

eTMF systems

Job description

Predicine, located in Hayward, CA, is seeking a Clinical Trial Associate to support the planning, execution, and operational management of global clinical trials, working with cross-functional teams, sites, investigators, CROs and sponsors to ensure studies are conducted efficiently and in compliance with GCP and company procedures.

The ideal candidate is highly organized, detail-oriented, proactive, and able to manage multiple priorities in a fast-paced environment, with excellent communication