Senior Clinical Scientist - Onsite Trials Lead

Abbott (abbottcareers2 board); Los Angeles (CA); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Free medical coverage for employees

Retirement plan with high employer con

Tuition reimbursement

FreeU education benefit

Job summary

Abbott in Sylmar, CA is seeking a Senior Clinical Scientist for an onsite role. The position focuses on independent clinical study planning and execution, ensuring adherence to GCP, regulatory standards, and SOPs.

You will manage essential documents, data corrections, AE trends, and protocol deviations. Responsibilities include developing study materials, coordinating start-up and maintenance of sites, and mentoring less experienced team members while collaborating with vendors and internal

Responsibilities

• Ensures regulatory and clinical protocol compliance for all assigned clinical projects.
• Drafts study materials such as patient brochures, recruitment material, presentations; drafts protocol summaries and annual reports.
• Drafts informed consent documents and case report forms with edit logic; assists with site nomination and selection.
• Coordinates start-up and maintenance of clinical study sites; leads activities with committees, vendors, and core labs.
• Reviews site compliance and raises issues to study management; may lead meetings on compliance concerns.
• Reviews and processes product complaints and adverse events; drafts serious adverse event narratives.

Job description

Abbott in Sylmar, CA is seeking a Senior Clinical Scientist for an onsite role. The position focuses on independent clinical study planning and execution, ensuring adherence to GCP, regulatory standards, and SOPs.

You will manage essential documents, data corrections, AE trends, and protocol deviations. Responsibilities include developing study materials, coordinating start-up and maintenance of sites, and mentoring less experienced team members while collaborating with vendors and internal